Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 1 minute ago
CanadaCardinal Health Cardiac Electrophysiology (EP) Packs
Cardinal Health was recently informed of a medical device recall from Medline Industries.Medline Namic Angiographic Control Syringes
The Namic RA syringes have been recalled by Medline due to a potential risk of the syringe rotating adaptor unwinding during use.HIZENTRA: The appearance is out of specification in the affected lot.
The appearance is out of specification in the affected lot.
Unauthorized and counterfeit health products seized at Thumbs Up 4 Shiatsu in Mississauga may pose serious health risks
Health Canada is warning consumers about multiple unauthorized and counterfeit health products seized at Thumbs Up 4 Shiatsu in Mississauga, Ontario.
United StatesBaxter Healthcare Corporation recalls Brand Name: Welch Allyn
Display screen may unintentionally flicker due to a software issue.Abbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version…
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.Hologic, Inc. recalls Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585…
Due to product exhibiting potential to generate either invalid or false negative results.Stryker Medical Division of Stryker Corporation recalls Cub Pediatric Crib
Cribs sold in the USA are missing two access door warning labels.LeMaitre Vascular, Inc. recalls Artegraft Vascular Graft
Labeling mix-up resulting in the incorrect lot outer packaging of product.ConvaTec, Inc recalls Convatec and 2 more products
Drainable large pouch may leak due to manufacturing issue.Diagnostica Stago, Inc. recalls Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF…
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1 and 2 more products
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer.Elekta, Inc. recalls Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion…
Due to adapter not being properly aligned or locked in place.Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment.Datascope Corp. recalls Battery Charging Station
The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP.Somerset Therapeutics LLC recalls Dexamethasone Sodium Phosphate Injection
Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for…Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad
Non-Sterility: microbial contamination identified as Paenibacillus phoenicisAnnora Pharma Private Limited recalls Pitavastatin Tablets
Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mgStrides Pharma Inc recalls Children's Ibuprofen Oral Suspension
Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 0.2%/0.5%*
Lack of Assurance of SterilityOlympus HF Cable
Olympus received a complaint involving a thermal event with an HF cable during a procedure, causing a user burn.iVascular Navitian
A potential risk has been identified through post-market surveillance: deterioration of the outer layer of the thinner distal segment of the device, which could lead to…Ortho Connect
A potential safety issue was reported of incorrectly releasing discrepant test results to a healthcare environment identified under very specific conditions.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.