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 StatesPhilips Medical Systems Nederland B.V. recalls Product Name: Allura Xper FD10C and 15 more products
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or…Hangzhou Bever Medical Devices Co., LTD. recalls BD Ready-to-Use Hydrophilic Catheter 14 Fr
Labeling error, Incorrect expiration dateIntuitive Surgical, Inc. recalls da Vinci SP
Access Port System tray may develop cracks potentially resulting in a sterility breach.Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS and 5 more products
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery…Canon Medical System, USA, INC. recalls VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 and 1 more products
There is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems.Elekta, Inc. recalls MOSAIQ Oncology Information System with Particle Therapy License
Using oncology information system that manages workflow may result in overtreatment if:Plan delivered with Particle Therapy IHE-RO TDW-II interface,With one field per…Sun Pharmaceutical Industries Inc recalls Clindamycin Phosphate USP
Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.Alvogen, Inc recalls Levothyroxine Sodium Tablets
Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.Advanced Pharmaceutical Technology, Inc. recalls TESTO-100 CIII
Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.Cipla USA, Inc. recalls Lanreotide Injection
Presence of Particulate Matter.Encon Safety Products Co recalls AQ 120 GFEW
cGMP deviations.Sun Pharmaceutical Industries Inc recalls Fluocinolone Acetonide Solution Topical Solution USP
Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D.Gold Star Distribution Inc recalls Advil a) Ibuprofen and 26 more products
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
CanadaHickmanâ„¢ and Broviacâ„¢ Central Venous Catheter Kits
BD has identified via internal inspections that the packaging of some Hickman catheter and Broviac catheter kits may have damage present on the outer tray, potentially…Omni Legend
Potential for image artifact on certain Omni Legend system images.Prismaflex Control Units
Vantive is issuing an urgent medical device correction to all Prismaflex control unit users due to the potential dislodgement of the Prismaflex Set deaeration chamber…ShockPulse-Se Lithotripsy System and ShockPulse Lithotripsy Generator
Olympus discovered through an internal investigation that specific serial numbers of ShockPulse generators may have a mis-wired component.Hamilton-C2 Intensive Care Ventilator
Hamilton Medical AG became aware of a malfunction with HAMILTON-C2 ventilators when used long term with neonatal patients.BiOptimizers Magnesium Breakthrough capsules; Residue on capsules
Affected lot contains small amounts of residue found on some capsules in bottles.Olympus Resection and Inner Sheaths
Olympus has identified complaints related to the ceramic tip of the resection/inner sheath breaking.Aesculap unlicenced medical devices
Internal review found 82 medical devices imported to Canada without an appropriate license by Health Canada.
Updated: Great White North Growers Inc. recalls certain Lunaire brand dried cannabis products due to heavy metal contamination
The affected lots contain arsenic, a toxic heavy metal, at levels above the acceptable limit.A.T.S.® 5000TS (Tourniquet System) With Hoses And Lop Sensor (Personalized Pressure)
Zimmer Biomet is conducting a phased serial specific medical device recall for A.T.S.A little guidance
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