Medical device recalls (page 11)
2545 recalls.
- A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - Short Monobloc Stem Broaches recall (Medacta Usa Inc)
Medical deviceClass IIReported July 8, 2026 · Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the... - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported July 8, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported July 8, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - 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... - SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 ... recall (Mentor Texas LP)
Medical deviceClass IIReported July 8, 2026 · A single lot of expired syringes were distributed due to a distribution system control failure. - 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... - Omnipod recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.... recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA P.CIRCUIT 5KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - 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... - Breathing circuit set recall (Hamilton Medical AG)
Medical deviceClass IReported July 8, 2026 · Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which... - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - 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. - Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 1, 2026 · There is the potential for leakage along the drug pathway from the pump through the end of the catheter. - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿... recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package. - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US... recall (Dexcom, Inc.)
Medical deviceClass IIReported July 1, 2026 · Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were... - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. recall (IPG Medical Corporation)
Medical deviceClass IIReported July 1, 2026 · Software anomaly that causes a false display of error code 5018. - GE Healthcare AW Server 3.2 ext.6.5 recall (GE Medical Systems SCS)
Medical deviceClass IIReported July 1, 2026 · GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client... - INZONE DETACHMENT SYSTEM recall (Stryker Neurovascular)
Medical deviceClass IIReported July 1, 2026 · Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and... - Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe... recall (Acumed LLC)
Medical deviceClass IIReported July 1, 2026 · Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System Small recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Multi-Snare Set: 5 mm x 125 cm recall (PFM MEDICAL INC.)
Medical deviceClass IIReported July 1, 2026 · A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility... - VOCSN+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported July 1, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which... - TMJ Bilateral Implants recall (TMJ Solutions Inc)
Medical deviceClass IIReported July 1, 2026 · Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Da Vinci ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported July 1, 2026 · Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would...