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 StatesAjanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules and 2 more products
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.CareFusion 213, LLC recalls BD PurPrep and 1 more products
Lack of assurance of Sterility: potential product contaminationCentral Admixture Pharmacy Services, Inc (CAPS) Los Angeles recalls TPN bag
Incorrect Product Formulation: product did not contain insulin as listed in the label.Zimmer, Inc. recalls Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula…
Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals.Clinical Innovations, LLC recalls Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery…
Due to complaints of device breakage at the traction force gauge to handle joint.Siemens Healthcare Diagnostics Inc recalls epoc BGEM BUN Test Card
Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous…Immuno-Mycologics, Inc recalls Immy
Neutralization Buffer may contain contaminantsMerit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098B Sterile EO and 1 more products
catheter may experience resistance when being advanced over the guidewireHealthmark Industries Co., Inc. recalls Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style
Product does not have FDA clearance.Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak…
The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin…North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices…
Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error…Elekta, Inc. recalls Brand Name: Leksell Vantage Arc System REF: 1053958
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.Abbott Point Of Care Inc. recalls i-STAT EG7+ cartridge and 2 more products
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge…Straumann USA LLC recalls Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304.… and 1 more products
Includes an incorrect screw seat interface.Siemens Healthcare Diagnostics, Inc. recalls Dimension Creatinine Flex reagent cartridge. Material Number: 10872079.
Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the…Beta Bionics, Inc. recalls iLet Bionic Pancreas
insulin pump software versions 1.4.2, and 1.4.3 issue with Dexcom Continuous Glucose Monitoring (CGM) G7 sensor may result in delayed CGM reading then switch to non-CGM…Milestone S.R.L. recalls VACUUM BAG SU LARGE
There is a possibility of reagent leakage from the specimen container.Depuy (Ireland) recalls Depuy Synthes and 8 more products
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.Heraeus Medical GmbH (Dental Division) recalls Heraeus and 1 more products
Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock…Medtronic, Inc. recalls Medtronic Sphere-9 Catheter
Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter…Whill, Inc. recalls WHILL Model C2 and 1 more products
Cyber vulnerability of BLE communication was found by CISA VDP program.Medline Industries, LP recalls Centurion medical convenience kits and 6 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads.Boston Scientific Corporation recalls Boston Scientific Pacemaker and 1 more products
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers…A little guidance
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