Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 19 minutes ago
United States2026 E-Series and other models recall: Incorrect cargo carrying capacity on label
Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.2024-2025 Freightliner Business Class M2 recall: Insufficient oil in steering gear box may cause gears to bind
A lack of lubrication may cause binding gears and difficulty steering, increasing the risk of a crash.CareFusion 303, Inc. recalls BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System…
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital…Elekta, Inc. recalls Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy
Due to a manufacturing issue and electrical grounding of systems.NIPRO Technical Services, Inc. recalls Conductivity Standard Solution Catalog/Model Numbers: 10001
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for…LimFlow, Inc. recalls Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Incorrect expiration dateCanon Medical System, USA, INC. recalls Alphenix INFX-8000C and 3 more products
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray…Cerapedics, 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.A little guidance
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