Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 4 minutes ago
United StatesMaquet Cardiovascular, LLC recalls The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run…Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula and 1 more products
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.Medline Industries, LP recalls Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267 and 1 more products
Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach.Tosoh Bioscience Inc recalls ST AIA-Pack Testosterone
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause…Argon Medical Devices, Inc recalls Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F and 5 more products
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.Oscor Inc. recalls Abiomed REF: 0052-3025 and 2 more products
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines…Olympus Corporation of the Americas recalls Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. and 3 more products
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the…GE Medical Systems, LLC recalls Optima XR200amx and 2 more products
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may…Daavlin Distributing Company recalls Photera 400 and 2 more products
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of…ICU Medical, Inc. recalls ICU Medical Plum Duo Infusion Pump and 1 more products
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the…Papablic Inc recalls Papablic Replacement Brush Heads. Model Number: Papablic18B and 1 more products
Potential for brush heads to break.Abiomed, Inc. recalls ABIOMED Impella RP Flex with SmartAssist Set and 12 more products
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers.Boston Scientific Corporation recalls Rapid Refill Continuous Injection System
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor.Orthofix U.S. LLC recalls Orthofix MINIRAIL and 3 more products
Unilateral external fixation devices may be incorrectly labeled.Padagis US LLC recalls Nystatin Cream USP
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.CareFusion 213, LLC recalls BD ChloraPrep Clear
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicatorBell Pharmaceuticals, Inc recalls CVS Health and 10 more products
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).Chiesi USA, Inc. recalls CLEVIPREX
Lack of Assurance of Sterility
CanadaCardinal Health - Presource® Kits Containing the Ritmed® Neurological Sponges
Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed® Neurological Sponges referenced.Shimadzu X-ray High Voltage Generators
Shimadzu Corporation has identified a potential issue in the X-ray High Voltage Generator.Atellica® CH Urine Albumin (UAlb)
Siemens Healthineers has confirmed, through the investigation of customer complaints, the potential for the following issues associated with processing Atellica CH…ER-Spec Single-Use Vaginal Speculum with LED Light Source
Units from specific lots of the ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small, may exhibit a plastic burr on the proximal plastic blade, near the…Merge PACS
Merge PACS Dynamic Thumbnail Refresh feature may cause thumbnails from a previously opened patient study to display in the Thumbnail Bar of a different patient's study.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.