Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 11 minutes ago
CanadaCheckcell®
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…Medline Hudson RCI Medium Concentration Oxygen Masks
Medline received complaints regarding the tubing disconnecting from the oxygen mask.
United StatesDICOM Grid, Inc. recalls Intelerad InteleShare software
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in…Medline Industries, LP recalls SCISSORS and 1 more products
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.Medtronic MiniMed, Inc. recalls InPen App
When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow…Seaspine Orthopedics Corporation recalls Orthofix NorthStar OCT Navigation Surgical Technique Guide
The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with…Copan Italia recalls 1ml of DTT in liquid phase and 1 more products
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.Fresenius Medical Care Holdings, Inc. recalls 5008X CAREsystem +CLiC +CDX
Several software anomalies with the potential to impact patient treatment, of which one includes the possibility to result in treatment stop if certain conditions are…Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.Dsaart LLC recalls Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant… and 5 more products
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system and 2 more products
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in…Datascope Corp. recalls Cardiosave Hybrid and 1 more products
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.GE Healthcare GmbH recalls GE HealthCare ViewPoint 6
GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical…Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray… and 5 more products
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.AVID Medical, Inc. recalls Halyard and 4 more products
Potential for incomplete seal on header bag.Abbott Laboratories recalls Alinity ci-series System Control Module
Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction.A little guidance
Get more from your tools
Practical guide 3 min read
Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
Practical guide 3 min read
How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
Practical guide 3 min read
What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.