Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 10 minutes ago
United StatesZydus Pharmaceuticals (USA) Inc recalls Icosapent Ethyl Capsules
Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.
CanadaDisinfectant Spray & Wipe Cleaner: Affected lots contain solution that do not meet the labelled strength
Affected lots contain solution that do not meet the labelled strength.Allura Xper and Azurion Systems
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch due to: cable or connector damage…Olympus Medical PK/PKS/Everest Cutting Forceps
Olympus identified inadequate supplier welding validation on several 5 mm cutting forceps models, which may cause jaw breakage during clinical use.RAPIDPoint® 500 Blood Gas Systems
Siemens Healthineers has confirmed that a limited number of Measurement Cartridge experienced exposure to temperatures below the specified storage conditions during…Approach® CTO Micro Wire Guide, Blue Rhino® G2-Multi Percutaneous Tracheostomy Introducer Set, Wayne Pneumothorax Set, Cook Spectrum® Central Venous Catheter Sets
Devices from the affected device lots have labels that state the incorrect expiration dates.GEM PAKs for the GEM Premier 5000 with iQM2
The company confirmed customer complaints indicating that specific GEM PAKs (cartridges) for the Gem Premier 5000 may experience an increased incidence of "Process…
Clore Beauty Supply products recalled due to missing mandatory hazard labelling
The recalled products do not have mandatory hazard labelling as required by the Cosmetic Regulations under the Food and Drugs Act, or the Consumer Chemical and…Instinct® Plus Endoscopic Clipping Device
Cook Medical has received 486 complaints of a malfunction that occurs when the user attempts to open the clip jaws by actuating the handle.Monojectâ„¢ 1mL Luer Lock Syringe, Tuberculin Print, Sterile
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however, the syringes contained within…SOLTIVE Premium SuperPulsed Laser System
Olympus received 98 complaints of sudden power loss or failure to power on in SOLTIVE superpulsed Laser System due to a defect in the 24V power supply.Arjo Tenor Mobile Lift
A supplier‑related brake component defect in the Tenor lift actuator may cause loss of self‑locking and sudden uncontrolled descent under load.
United KingdomHania Bridal Henna Paste safety warning
The product presents a serious chemical risk due to the presence of phenol.Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected product(s) are sold for inhalation without market authorization (DIN) in Canada.
Salt of the Earth Cedar and Amyris Replenish Cream recalled due to a chemical hazard
Health Canada’s sampling and evaluation program has determined that the recalled products contain methyl eugenol above the maximum concentration outlined in the…
Nextleaf Labs Ltd. recalls Glacial Gold – Anytime 1:1 Fuzzy Mango due to packaging and labelling issue
The affected products are packaged in the wrong pack.Advanced Bionics, LLC recalls Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor…
Behind-the-ear sound processer packaging label is different then included product.Olympus Corporation of the Americas recalls Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name…
Mis-wired component-the improperly wired component can result in additional noise on the power supply output.Vascutek, Ltd. recalls Gelsoft Plus
Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life.Diagnostica Stago, Inc. recalls Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S…
The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Urine Albumin
Falsely depressed UAlb patient results may occur.Datascope Corp. recalls CS100 IABP. Software Version CS100 IABP Q.01. and 1 more products
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.GE Healthcare recalls GE Healthcare Centricity Universal Viewer Zero Footprint Client
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with…A little guidance
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