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 StatesSheathing Technologies Inc recalls Sheathes3D Seamless Viral Barrier
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.Shenzhen Atomstack Technologies recalls Material Processing Laser Products
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)Ferndale Laboratories, Inc. recalls Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number…
Butyrate tube cracks during actuation, rendering product unusable.Philips Ultrasound, LLC recalls Philips EPIQ Ultrasound Systems
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.Beaver-Visitec International, Inc. recalls BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as…CareFusion 213, LLC recalls BD ChloraPrep" Triple Swabsticks
Lack of Assurance of SterlityNovo Nordisk Inc. recalls Wegovy and 1 more products
Presence of Particulate Matter: Hair was found in a prefilled syringeGlenmark Pharmaceuticals Inc., USA recalls Ondansetron Orally Disintegrating Tablets
Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out.Zydus Pharmaceuticals (USA) Inc recalls traZODONE Hydrochloride Tablets
Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.Indian Cookware And Appliance LLC recalls ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIA
Potential contamination due to leachable lead.Bendon Publishing recalls 1) Paw Patrol Heart-Shaped Gummy Candies
Unapproved color additive - chlorophyllin copper complexTom Bumble LLC recalls Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Chocolate GF V. Product is…
Foreign material.2026 Vision and other models recall: Wheelchair restraint retractor may not lock
An unsecured wheelchair can move during transit, increasing the risk of injury.2022-2024 All American transit buses recall: Loose 12-Volt cable may cause loss of drive power and electrical system
A loss of brake assist, drive power, steering assist, or instrument panel displays can increase the risk of a crash.2022-2025 R1S and other models recall: Toe link joint may separate
The toe link joint may separate, increasing the risk of a crash.LS2 Rebellion helmets and other models recall: Helmets may not adequately protect User/FMVSS 218
A helmet that does not provide adequate protection increases the risk of injury during a crash.2025 EX30 recall: Park outside - high voltage battery fire risk
A high-voltage battery that overheats increases the risk of a fire.2021-2026 Chief XL I and other models recall: Electrical systems may fail
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash.Alcon Research LLC recalls Brand Name: Alcon Laboratories
Ophthalmic procedure packs may have incomplete seals affecting sterility.Beckman Coulter Ireland, Inc. recalls BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system…
Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.AGFA Healthcare Corp. recalls Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common…
It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams.ICU Medical, Inc. recalls LifeShield Drug Library Management
Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001).A little guidance
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