Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 4 minutes ago
United Kingdom
CanadaAPO-BRIMONIDINE-TIMOP: The weight is out of specification in the affected lot.
The weight is out of specification in the affected lot.Chromophare Surgical Lighting System
Stryker has discovered that certain lots of the soffit ring may not adequately support the weight of the ceiling cover.Lifeworks Technology Vibra-Heal and Restore Massage Guns
The device was distributed in Canada without a valid class II Medical Device Licence under the Medical Devices Regulations.Olympus MAJ-1443 and MAJ-1444 Valves
Olympus is informing that the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OERPro and OER-Elite automated endoscope reprocessors.FDR Visionary Suite
Potential safety issue with the X-ray high voltage generator incorporated into the FDR Visionary Suite X-ray diagnostic equipment.Madsen® AccuScreen® TEOAE/DPOAE/ABR Probe
There is already an inherent risk of a false pass with the DPOAE testing protocol with AccuScreen® for a child with a hearing disorder and this cannot be eliminated.Abiomed Purge Cassette Generation 1 for Impella
Abiomed, Inc.
Essencia Basil and Essencia Bay Laurel essential oils recalled due to chemical hazard
Health Canada's sampling and evaluation program has determined that the recalled product contains methyl eugenol above the maximum concentration in the Cosmetic…Importation of US-Authorized Vasopressin Injection, USP, 20 units/mL (For IV Infusion) Due to the Current Shortage of Canadian-Authorized Vasopressin Injection, USP, 20 units/mL (For IM or SC Administration)
There is a shortage of Vasopressin Injection, USP, 20 units/mL (for intramuscular [IM] or subcutaneous [SC] administration) in Canada.
United StatesAgiliti Health - Ellis recalls Adapt Pump
Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management…Olympus Corporation of the Americas recalls Olympus Cystoscope Outer Sheath
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.Remel, Inc recalls Campy CVA Medium 100/PK
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.Edermy LLC recalls PIE Trolley System Model: 2005 and 1 more products
Lack of 510K clearanceHitachi, Ltd. Radiation Oncology Systems, Kashiwanoha recalls Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR and 1 more products
Software anomaly in the patient positioning system may result in positional discrepancy.Medline Industries, LP recalls Medline Sterile Saline Wound Wash and 4 more products
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level…Medtronic Perfusion Systems recalls Octopus Nuvo Tissue Stabilizer
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned.MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved…
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.Encore Medical, LP recalls Brand Name: Reverse Shoulder Prosthesis and 2 more products
Knee and Humeral socket implants contain incorrect labeling.Olympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and… and 19 more products
Complaints of the ceramic tip of the resection sheath breaking have been received.Medline Industries, LP recalls Medline Kits containing Tego Connectors: Medline IR Pack and 5 more products
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits.Agebox recalls Agebox iKids-Growth and 1 more products
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamorenLeo Pharma Inc recalls Adbry
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.AvKARE recalls Amantadine HCl
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.A little guidance
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