Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 0 minutes ago
United StatesBeckman Coulter Ireland, Inc. recalls BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system…
Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.AGFA Healthcare Corp. recalls Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common…
It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams.ICU Medical, Inc. recalls LifeShield Drug Library Management
Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001).Intuitive Surgical, Inc. recalls da Vinci 5
Surgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable Ergonomics: Viewer…Diasol, Inc recalls Brand Name: Diasol Product Name: 100225-10-DEX100 and 5 more products
Safety and efficacy of dialysis acid concentrate cannot be assuredMicrobiologics Inc recalls KWIK-STIK 2-Pack and 2 more products
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp.Cook Incorporated recalls Flexor Check-Flo Introducers and Sets and 2 more products
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.Draeger, Inc. recalls Draeger Vapor 2000. Unheated and 1 more products
A certain component of affected devices was not delivered within specification and contained impurities.Howmedica Osteonics Corp. recalls The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed…
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application"…ICU Medical, Inc. recalls LifeShield Drug Library Management
For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed.Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… and 16 more products
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.Medtronic Neuromodulation recalls Restore Clinician Programmer Application
Software issue where a Device Reset message displayed on the app was unable to be cleared.CareFusion 303, Inc. recalls BD Pyxis MedStation ES
Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a…Merck Sharp & Dohme LLC recalls Merck Emend and 1 more products
Presence of particulate matter: potential presence of metal particulates in the product.
CanadaMedline Homecare Beds
Medline identified the following two risks with Medline homecare beds through post-market surveillance: (1) electrical system safety risks which may result in fire and…Checkcell®
Some vials of Checkcell lot 43257 exhibited clot formation, hemolysis, and unexpected darkening of the red blood cells.Codman Microsensor® Basic Kits and CereLink™ ICP Sensor Basic Kits
During an investigation, Integra Lifesciences identified lots that were released with potential corrosion stains on the surface of the 14-gauge tuohy needle that is…CellMek SPS
Beckman Coulter has confirmed an error in SW version 2.3.90.0 that causes samples to be dispensed unexpectedly close to the bottom of the output tubes.TEGO Connector
ICU Medical has identified lot-specific issues with the silicone seal on the TEGO device.Olympus Single Use Electrosurgical Knives
Olympus determined that deterioration of the cutting knife, caused by overheating and burning, can contribute to tip breakage during use.Azurion R2.1.10 and R2.2.10 systems
Philips has identified six software issues affecting Azurion R2.1.10 and R2.2.10 systems that may result in loss of imaging (x-ray) functionality, and/or loss of…Unauthorized health products seized from two stores in Maple Ridge, BC may pose serious health risks
Health Canada is warning consumers about multiple unauthorized drug products seized at two retail locations in Maple Ridge, British Columbia: Maxximus Supplements…Unauthorized health products sold online and seized at Rize Fitness may pose serious health risks
Health Canada is warning consumers about multiple unauthorized health products seized from Rize Fitness located at 188 Smithe Street, in Vancouver, British Columbia…A little guidance
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