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 2 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.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).Intuitive Surgical, Inc. recalls da Vinci 5
Surgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable Ergonomics: Viewer…Diasol, Inc recalls Brand Name: Diasol Product Name: 100225-10-DEX100 and 5 more products
Safety and efficacy of dialysis acid concentrate cannot be assuredMicrobiologics Inc recalls KWIK-STIK 2-Pack and 2 more products
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp.Cook Incorporated recalls Flexor Check-Flo Introducers and Sets and 2 more products
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.Draeger, Inc. recalls Draeger Vapor 2000. Unheated and 1 more products
A certain component of affected devices was not delivered within specification and contained impurities.Howmedica Osteonics Corp. recalls The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed…
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application"…ICU Medical, Inc. recalls LifeShield Drug Library Management
For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed.Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… and 16 more products
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.Medtronic Neuromodulation recalls Restore Clinician Programmer Application
Software issue where a Device Reset message displayed on the app was unable to be cleared.A little guidance
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