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 24 minutes ago
United StatesGrace Medical, Inc. recalls TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product…
Due to incorrect functional length on device labeling.Siemens Medical Solutions USA, Inc recalls ARTIS pheno and 1 more products
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient.Covidien LLC recalls COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code…
Due to customer complaint regarding incorrect display box labeling.Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid…
Due to incorrect shelf-life expiration date.GE Medical Systems China Co., Ltd. recalls MAC 5 A4 Resting ECG Analysis System 855001-001
Software in development inadvertently made available for customer use.Daavlin Distributing Company recalls Phothera 200
Some of the Calibration/Output Certificates had the outputs reversed.Kayserbetten GMBH & Co. KG recalls Pediatric care bed
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an…Stryker Corporation recalls Neptune Smart Docking Station
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior…Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set and 1 more products
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when…Bayer Medical Care, Inc. recalls Avanta Multi-Patient Administration Tube Sets
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System.CareFusion 303, Inc. recalls BD Pyxis MedStation 4000 REF: 303 Medication cabinet and 7 more products
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.Draeger, Inc. recalls Atlan A350. Model Number: 8211500. anesthesia workstation and 1 more products
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.Covidien LLC recalls Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 and 2 more products
Temperature probe devices lack FDA clearance.B Braun Medical Inc recalls Spinal Needle procedure kits: Material Description and 2 more products
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP.Becton Dickinson & Company recalls BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in. and 9 more products
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP.Philips Medical Systems Nederland B.V. recalls Philips Azurion 3M12 and 7 more products
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable.B Braun Medical Inc recalls Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY… and 7 more products
B.Lannett Company Inc. recalls Niacin Extended-release Tablets
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.Asclemed USA Inc. recalls Duloxetine DR Capsules
CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications: Olmesartan Medoxomil content below specificationsSun Pharmaceutical Industries Inc recalls Xyvona and 1 more products
Labeling: Not Elsewhere Classified.Eugia US LLC recalls Lidocaine HCl Injection
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scanA little guidance
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