Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 25 minutes ago
Canada
United KingdomQ3 Nail Dust Collector sold via Amazon safety warning
The product presents a serious risk of fire as the creepage and clearance distances are insufficient.InteleShare™
The length measurement tool may provide inaccurate values when used in multi-planar reconstruction when rotations are applied.CranialMask Tracker
Stryker has discovered an issue where the Cranial Guidance Software may generate the following error message: "Instrument 'Face Mask (6001385000000) is not valid for…Coulter DxH Diluent
Beckman Coulter has confirmed that specific diluent lot numbers of Coulter DxH Diluent contribute to elevated platelet (PLT) Daily Checks background counts cycle when…Philips Lumify Systems
Philips has become aware that the Lumify system is incompatible with Apple devices that have USB-C connector and are running iOS 18, which will cause a failure to…MapleLife Magnesium Bisglycinate 200mg: Undeclared ingredient (Magnesium Oxide)
Label non-compliance: undeclared source of medicinal Ingredient: Magnesium Oxide.
Various Everpro Gray Away products recalled due to missing mandatory hazard labelling
These products do not meet the Cosmetic Regulations in Canada.
United StatesMerit Medical Systems, Inc. recalls PhD Hemostasis Valve
Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience…Medline Industries, LP recalls MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.Elekta Solutions Ab recalls MOSAIQ Oncology Information System Software Builds 3.1.3
When appending a care plan that contains one or more wave medication orders, the occurrence and frequency of the appended orders may not match the intended schedule.Auris Health, Inc recalls MONARCH Bronchoscope. Model Number: MBR-000211-B
Potential that product was leak tested with equipment outside of its expected operating range, resulting in bronchoscopes that may not be susceptible to leaks.Sterilmed, Inc. recalls Brand Name: ACUSON and 1 more products
Affected catheters were reprocessed beyond validated cycles.Beckman Coulter Inc. recalls DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The DxFLEX Flow…
Due to a software error code that crashes during acquisition on patient sample when running customer defined acquisition protocol.Berkeley Advanced Biomaterials, LLC recalls Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code:
Due to incorrect product label (Incorrect product name identified on outer packaging).Becton Dickinson & Company recalls BD Luer Tip Caps
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.Quest International, Inc. recalls Brand Name: ReQuest Measles IgG Product Name: Rubeola IgG Enzyme Linked Immunoabsorbant…
Due to distributing the measles IgG IVD without a premarket approved/cleared.TMJ Solutions Inc recalls TMJ Bilateral Implant REF: CHG020 Sterile EO
Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.Greiner Bio-One North America, Inc. recalls Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog…
Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were manufactured without gel separator, which could yield erroneous assay results and require the…Medtronic Perfusion Systems recalls MC3 VitalFlow Console
As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation.Olympus Corporation of the Americas recalls Brand Name: EZDilate Nephrostomy Balloon Catheter and Inflation Device Kit Product Name…
Device kits contained an incorrectly sized 4mm x 4cm urinary tract balloon catheter (BURS0404) instead of the correct 8mm x 15cm nephrostomy tract balloon catheter…Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC recalls OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials…
A labeling error was identified on the affected product.Medtronic Perfusion Systems recalls Medtronic HR-ACT
Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.Meridian Bioscience Inc recalls Meridian Bioscience and 1 more products
The cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.A little guidance
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