Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 4 minutes ago
United StatesCerapedics, Inc. recalls PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft
Incorrect expiration dateGold Star Distribution Inc recalls Bandages and first aid kits: FIRST AID KIT 24/42PC and 4 more products
Potential exposure of rodents and rodent activity in the distribution center.Cardinal Health 200, LLC recalls Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal…
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems… and 1 more products
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings.Miach Orthopaedics recalls BEAR Implant. Model Number: 1000.
Incorrect expiration date on label that extends beyond the product's documented/approved shelf life.SunMed Holdings, LLC recalls Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape… and 3 more products
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R and 1 more products
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous…Philips North America recalls Evolution Upgrade 1.5T. Product Codes and 12 more products
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).Aju Pharm Co., Ltd. recalls Fixone Hybrid Anchor and 7 more products
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2 and 14 more products
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during…LSL Healthcare Inc. recalls LSL Healthcare
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.Sato Pharmaceutical Co., Ltd recalls INON ACE Antacid tablets
Failed Disintegration Specifications: above the time expected.Greenstone Llc recalls methylprednisolone tablets
Labeling: Not Elsewhere Classified.Novadoz Pharmaceuticals LLC recalls Glycopyrrolate Oral Solution
Failed Impurities/Degradation SpecificationsBaxter Healthcare Corporation recalls Sterile Water for Irrigation
Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solutionHaleon US Holdings LLC recalls parodontax
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
Mindbodygreen Recalls Ultimate Multivitamin+ Dietary Supplement Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
The bottles are filled with dietary supplements containing iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.GVS TM, Inc recalls SQ40S Blood Transfusion Filter
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.Intuitive Surgical, Inc. recalls Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog…
Due to probe bags that may have a compromised or incomplete sterile pouch seal.Beckman Coulter Ireland, Inc. recalls The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique…
Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU).Mazor Robotics Ltd recalls Mazor X robotic guidance system REF: TPL0059
Software errors that can result in incorrect surgical instrument positioning during spinal surgery.Philips North America recalls Patient Information Center iX
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.Sysmex America, Inc. recalls TS-10/TS-10H Tube Sorter
Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift.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.