Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 9 minutes ago
United StatesElekta, 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…Philips North America recalls Philips Achieva 1.5T with MR Elastography and 18 more products
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the…Hologic, Inc recalls Brand Name: Genius" Review Station Product Name: Genius" Review Station Display
It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the…Medline Industries, LP recalls Medline Neuro Sponges and 30 more products
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product…Becton Dickinson & Co. recalls BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use and 1 more products
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon…American Regent, Inc. recalls Levocarnitine Injection
Labeling: Missing LabelWater-Jel Technologies, LLC recalls Lidocaine Wound Gel
Failed PH SpecificationsScope Health recalls Optase Dry Eye Intense Drops
Lack of Assurance of SterilityHikma Pharmaceuticals USA INC recalls Alendronate Sodium Oral Solution
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.Alcon Research LLC recalls Systane and 1 more products
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.Wells Pharma of Houston LLC recalls Phenylephrine Hydrochloride Injectable Solution and 6 more products
cGMP deviations.Thea Pharma, Inc. recalls iVIZIA and 1 more products
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.A little guidance
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