Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 13 minutes ago
United StatesMagellan Diagnostics, Inc. recalls and 2 more products
Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the…Arrow International, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: and 7 more products
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured Due to receiving a notice from a supplier that the liquid adhesive was…LSL Healthcare Inc. recalls LSL Healthcare and 5 more products
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be… and 11 more products
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode and 3 more products
Potential for detachment of a distal tip component of the device during use.Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes… and 16 more products
Unapproved design changes to the products outside of the 510(k) clearance.Medline Industries, LP recalls Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT and 21 more products
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter and 19 more products
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.Hetero Labs Limited (Unit V) recalls Pantoprazole Sodium
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."Teva Pharmaceuticals USA, Inc recalls Claravis
Failed Impurities/Degradation Specifications: Out of specification for specific impurity TretinoinPremier Dental Products Co recalls Premier
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).Leading Pharma, LLC recalls Furosemide Tablets
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.B Braun Medical Inc recalls Sterile Water for Injection USP and 3 more products
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.Harrow Eye LLC recalls FRESHKOTE LUBRICANT EYEDROPS
Lack of Assurance of SterilityThe Harvard Drug Group LLC recalls Omega-3-Acid
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
CanadaCook Medical Beacon® Tip Centimeter Sizing Catheter
Cook Medical identified that the marker bands on impacted products may be at an increased risk of cracking/breakage.Automated Impella® Controller
Abiomed, Inc.H2O: Presence of particulate matter in affected lot
Presence of particulate matter in affected lot.Polysorb Coated Braided Absorbable Single Stitch Reload For Use With The Endo Stitch And Sils Stitch Suturing Devices
On Jan 22 2026, holes were found in both the breather pouch and the foil.Medline Neuro Sponges
Medline kits containing neuro sponges are being recalled due to a potential out-of-specification for endotoxin for the neuro sponges.Chuck For Pins Hoffmann3 Universal For Ø4/5/6mm
Stryker confirmed that certain lots of Hoffman 3 Universal Pin Chucks contained inhomogeneous coating with out-of-specification coating thickness and color.Vectorflow Antegrade Catheterization Product
Teleflex has initiated a voluntary recall for certain lots of the above-mentioned products due to receipt of a supplier-initiated recall of the Merit 16f dual-valved…Harmonyair A-Series Surgical Lighting System
Steris identified through customer complaints that paint from the lighting system's light head may begin to peel or chip over time as a result of routine cleaning…A little guidance
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