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
CanadaNitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.
United KingdomNov'Max Anti Volume Keratin Hair Treatment recall
The product presents a serious chemical risk because it contains formaldehyde.Bondi Sands Zinc Mineral Sunscreen SPF50+ Body Lotion and Face Lotion recall
The product presents a risk to health because certain batches have shown signs of separation and uneven texture.Vacuum Bag SU Large
Leakage from the specimen container may occur.Soft-Vu and Accu-Vu 4 FR Angiographic Catheters
AngioDynamics, Inc., is conducting a voluntary medical device field safety corrective action or recall to the end-user level based on the non-conformance of a molded…
United StatesBoston Scientific Corporation recalls EndoVive Safety PEG Kit
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD.Lutronic Corporation recalls CLARITY II Laser System
Reports of devices sparking/popping and potentially burning patients.Medline Industries, LP recalls Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN and 1 more products
Fabric may experience premature delamination when using included laundering instructions.Ion Beam Applications S.A. recalls IBA Proton Therapy System
It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration.Becton Dickinson & Company recalls 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk…
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.Altruan GmbH recalls Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic… and 2 more products
Product not cleared by the FDA.Covidien LLC recalls HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product…
Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote patient…KOB GmbH recalls MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE
Due to labeling error.Medartis AG recalls Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm and 1 more products
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.Physio-Control, Inc. recalls PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers…
Due to pediatric defibrillator electrode delaminationExactech, Inc. recalls Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog… and 1 more products
Impactor handle may be missing cross-pinMedline Industries, LP recalls Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART
The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient…Raz Design Inc recalls Raz-AT
Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place.International Life Sciences recalls Artelon FlexBand Dynamic Matrix Ref: 31057 and 2 more products
Augmentation devices failed bacterial endotoxin testing.Trividia Health, Inc. recalls Owner's Booklets and Instructions for Use that are used with the following blood glucose… and 3 more products
The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code.Beckman Coulter Mishima K.K. recalls DxC 700 AU and 1 more products
A delay in results may occur.Instrumentation Laboratory recalls GEM Premier 5000 PAK and 19 more products
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not…Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa and 9 more products
The device does not bear a unique device identifier.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.