Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 24 minutes ago
Lannett Company Inc. recalls Dextroamphetamine Saccharate
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.McKesson recalls Gemcitabine Injection
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.Accord Biopharma Inc recalls IMULDOSA
Lack of assurance of Sterility:Accord Healthcare, Inc. recalls Levothyroxine Sodium Tablets
Subpotent DrugLupin Pharmaceuticals Inc. recalls prednisoLONE Acetate Ophthalmic Suspension
Presence of Foreign SubstanceSun Pharmaceutical Industries Inc recalls Fexofenadine Hydrochloride Tablets
Failed Impurities/Degradation SpecificationsAsclemed USA Inc. recalls Accucaine and 1 more products
Lack of Assurance of SterilityCipla USA, Inc. recalls Cinacalcet Hydrochloride Tablets and 2 more products
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).Lupin Pharmaceuticals Inc. recalls Glucagon Emergency Kit for Low Blood Sugar
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.CareFusion 213, LLC recalls BD ChloraPrep Hi-Lite Orange and 9 more products
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers…Blaine Labs Inc recalls Revitaderm Wound Care Gel and 7 more products
Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp CGMP Deviations: product…TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns
Health Canada is reviewing significant concerns regarding the data integrity of the pivotal ADVOCATE trial, which served as the primary efficacy study supporting the…JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)
The dissolution may be out of specification in the affected lot.Hotline IV Fluid Warmer System & Accessories
ICU Medical became aware of an increased likelihood of leakage in specific lots of L-70 Hotline Fluid Warming sets due to potentially inadequate solvent application at…Urinary Catheter Trays containing Cliniclean Pericare Wipes
Based on customer feedback, BD has identified that the Cliniclean Pericare Wipes provided within urinary catheter trays may be potentially contaminated with a lubricant…Intramedullary Bone Saw Blade Assembly
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Sawblade Assembly due to potential sterile barrier packaging…Hybrid Hydrophilic Microguidewire
Performance variability affecting the hydrophilic coating of Hybrid007 guidewires in specific lots may increase friction during microcatheter navigation.DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Beginning in April 2026, complaints were received regarding pinhole leaks in the wire-wound body of 22 Fr EOPA™ elongated one piece arterial cannulae and EOPA 3D™…Omni-Tract Surgical Retractor System
Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum…NephroMax High Pressure Nephrostomy Balloon Catheter
Boston Scientific is notifying you that the renal sheath for certain NephroMaxâ„¢ high pressure nephrostomy balloon catheters may be packaged in a reversed orientation.Fludeoxyglucose (18F) Injection; Cracked vial
Fludeoxyglucose (18F) vial containing 24.80 mL (30.23 GBq of the product) used to administered the drug to the patients was found to be broken at the bottom.LIFECODES LSA Class II
Werfen has identified that two beads within the LIFECODES LSA class II assay kit(s) may present different DQB1 specificities than previously understood: • Bead 42 /…WASPLab
Copan WASP SRL is performing a medical device product correction related to the WASPLab product.A little guidance
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