Recalls in Kentucky (page 27)
3954 recalls.
- Thermos Recalls 8.2 Million Stainless King Food Jars and Bottles Due to Serious Impact Injury and Laceration Hazards
Consumer productReported May 1, 2026 · If perishable food or beverages are stored in the container for an extended period of time, the stopper can forcefully eject when opened, which can result in... - CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton recall (Mondelez Global Llc)
FoodClass IIReported April 29, 2026 · Hard corn starch lumps were found in the product - Claravis recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported April 29, 2026 · Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin - LACTATED RINGER'S IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - 0.9 % SODIUM CHLORIDE IRRIGATION recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - DEXTROSE INJECTION USP recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - Sterile Water for Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed. - Omega-3-Acid recall (The Harvard Drug Group LLC)
DrugClass IIReported April 29, 2026 · Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells. - Premier recall (Premier Dental Products Co)
DrugClass IIIReported April 29, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14).... - FRESHKOTE LUBRICANT EYEDROPS recall (Harrow Eye LLC)
DrugClass IIReported April 29, 2026 · Lack of Assurance of Sterility - Furosemide Tablets recall (Leading Pharma, LLC)
DrugClass IIReported April 29, 2026 · CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit. - Pantoprazole Sodium recall (Hetero Labs Limited (Unit V))
DrugClass IIReported April 29, 2026 · Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots." - LSL Healthcare Wound Closure Tray recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - LSL Healthcare recall (LSL Healthcare Inc.)
Medical deviceClass IIReported April 29, 2026 · Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. - Sequencing Agent SEQ0067 recall (Foundation Medicine, Inc.)
Medical deviceClass IIReported April 29, 2026 · Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants - Flamingo Funnel Large recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Medium recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Flamingo Funnel Small recall (SurgiSmoke Solutions)
Medical deviceClass IIReported April 29, 2026 · Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. - Oxoid Agglutinating Sera recall (Remel Europe Ltd.)
Medical deviceClass IIReported April 29, 2026 · Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a... - Access Total T4 Calibrator recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported April 29, 2026 · Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Custom Convenience Kits Pre Op Kit - NS recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported April 29, 2026 · The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump... - Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 recall (Micro-X Ltd.)
Medical deviceClass IIReported April 29, 2026 · X-Ray generator may malfunction resulting in the X-Ray being inoperable. - Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr.... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - FLEXTIP PLUS EPIDURAL CATHETER recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured - Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IIReported April 29, 2026 · Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · XXX - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111 recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported April 29, 2026 · Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely. - nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft... recall (XTANT Medical Holdings, Inc)
Medical deviceClass IIReported April 29, 2026 · Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years. - Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog... recall (Davol, Inc.)
Medical deviceClass IIReported April 29, 2026 · Potential for product to contain foreign matter, confirmed to be inspect fragments. - LeadCare Ultra Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - LeadCare¿ Plus Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - (1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes... recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · Unapproved design changes to the products outside of the 510(k) clearance. - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - AccuVu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft -Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Soft-Vu Angiographic Catheter recall (Angiodynamics, Inc.)
Medical deviceClass IIReported April 29, 2026 · The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the... - Medline Kits: 1) ARTHROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) HYSTEROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) GYN LAPAROSCOPY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) LABOR PACK-22025208-LF recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) ARTHROGRAM TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) SYR CONTROL 8ML ROTATING recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) NEWBORN ADMISSION recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. - Medline Kits: 1) BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported April 29, 2026 · The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.