Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 17 minutes ago
United StatesBaxter Healthcare Corporation recalls Dextrose Injection
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.Ajanta Pharma USA Inc recalls Fluphenazine Hydrochloride Tablets
Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability.American Regent, Inc. recalls Epinephrine Injection
Presence of Particulate Matter and Lack of Assurance of Sterility.ImprimisRx NJ LLC recalls Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution
Subpotent DrugOurPharma LLC recalls fentaNYL Citrate
Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry…
CanadaOrganika® Gummies: Foreign site not listed on site licence
Affected lots were imported from a foreign manufacturing site not listed on the site licence.
Olli Brands Inc. recalls Olli StikiStix Multipack Sour Razzy Pink Lemonade (300 CBG 100 THC) due to labelling issues
The affected product has multiple labelling issues including missing information.
A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil
Product contains sildenafil and tadalafilTZIELD (teplizumab) and the Risk of Viral Reactivation
Serious and life-threatening cases of viral reactivation, including Epstein–Barr virus (EBV) and cytomegalovirus (CMV), have been reported with TZIELD.Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels
Elevated Endotoxin level
AustraliaColoured contact lenses designed for cosplay and makeup applications recall
The packaging solution for these contact lenses may be contaminated with Burkholderia cepacia complex bacteria.
Generic acetaminophen by Teva recalled because it may contain foreign material
Teva Canada Limited is recalling one lot of the non-prescription drug Novo-Gesic Forte 500 mg (acetaminophen) due to the potential presence of phenolic resin or epoxy…Centricity High Acuity Anesthesia
GE Healthcare has become aware of two potential issues associated with certain Centricity High Acuity (CHA) systems.Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Analyzer
Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples.IMN Screws System Advanced Locking Screw
Following a product complaint, and as part of its standard quality process, Stryker confirmed that one lot of T2 Alpha IMN advanced locking is incorrectly labeled.Veradius Unity and BV Pulsera Mobile C-Arm System-9in. and 12in. Versions
Air bubbles may develop in the monoblock oil when there is a prolonged period between manufacture and installation, for example due to storage, transportation, or other…Philips Ingenia, Achieva and Intera MR Systems
Philips has become aware of a software issue affecting Philips Magnetic Resonance (MR) imaging systems operating with software versions R5 & R11, which may terminate an…B Braun Medical Inc recalls Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number…
Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump and 1 more products
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI)…Fresenius Medical Care Renal Therapies Group, LLC recalls GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B and 2 more products
Complaints of blue-green discoloration in productMedos International Sarl recalls Velys Enabling Tech Robotic-Assist Station REF: 451611001
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear and 12 more products
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete…Philips North America Llc recalls Philips Brilliance. Models: Brilliance iCT and 3 more products
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the…A little guidance
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