Medline Industries, LP recalls (page 2)
524 recalls.
- Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline breathing circuits labeled as: 1) HUDSON RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline Hudson RCI recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline Micro-Kill Bleach Germicidal Bleach Wipes recall (Medline Industries, LP)
Medical deviceClass IIReported August 19, 2026 · Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled... - Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU... recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: 1) SHOULDER PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters recall (Medline Industries, LP)
Medical deviceClass IIReported July 29, 2026 · Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the... - MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to... - MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to... - MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose... - MEDLINE convenience kits labeled as: 1) C-SECTION recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose... - MEDLINE ANTERIOR HIP recall (Medline Industries, LP)
Medical deviceClass IReported July 29, 2026 · Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 22, 2026 · Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) OPEN HEART PEDS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF recall (Medline Industries, LP)
Medical deviceClass IIReported July 15, 2026 · Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the... - Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH recall (Medline Industries, LP)
Medical deviceClass IReported July 8, 2026 · Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on... - Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA -... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL LINE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURING SET recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) IMAGING BIOPSY TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) STD recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) DYNJ0621189X recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MULTIMED recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) BLOCK TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. KIT... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DYNJ905503F recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - MEDLINE Medical Procedure Kits labeled as: 1) CRANI recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) RETINA LAC/USC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BASIC GYN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: NURSING KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CH OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include...