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 25 minutes ago
United StatesElekta, Inc. recalls MOSAIQ Oncology Information System
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.HF Acquisition Co LLC recalls Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE and 1 more products
Due to incorrect incubation process being performed on product.The Binding Site Group, Ltd. recalls Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A…
It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured.AVID Medical, Inc. recalls Halyard and 3 more products
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.Fresh Roast Systems Inc recalls Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100
A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse…D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE" and 2 more products
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.Sagemax Bioceramics, Inc. recalls NexxZr T Multi A3.5 W98-16mm
Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's…Boston Scientific Neuromodulation Corporation recalls Boston Scientific Model SC-4318
Sterile anchors my lack sterility assurance.Micromed S.p.A. recalls SD LTM 64 PLUS
Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier…In2bones USA, LLC recalls NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name…
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.Boston Scientific Neuromodulation Corporation recalls Boston Scientific CSK Electrodes: REF: CSK-TC10 and 1 more products
Reusable electrodes may not meet expected performance levels.Mozarc Medical US LLC recalls Mahurkar Elite PASS Trays
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.Avanos Medical, Inc. recalls Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320 and 19 more products
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.Fresenius Medical Care Holdings, Inc. recalls Bicarby Dialysate
There is an error in the labeling of the GTIN on the product.GE Medical Systems, LLC recalls Allia IGS 3 Pulse angiographic X-ray system and 4 more products
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators.INSPIREMD Inc recalls Brand Name: CGuard¿ Prime Carotid Stent System and 5 more products
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.Golden State Medical Supply Inc. recalls GSMS Incorporated
Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour…Amneal Pharmaceuticals, LLC recalls Primidone Tablets
Cross Contamination with Other Products: due to a potential for cross-contamination with Acemetacin API due to an issue at the API manufacturer.Sun Pharmaceutical Industries Inc recalls DOXOrubin Hydrochloride Liposome injection
Presence of Particulate matter: Particulate matter identified as glass.Fresenius Kabi USA, LLC recalls Epinephrine Injection
Failed Impurities/Degradations SpecificationsBreckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules and 1 more products
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limitZep Inc recalls Zep
Microbial contamination of sterile productsSun Pharmaceutical Industries Inc recalls Budesonide Inhalation Suspension
Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule…A little guidance
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