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 0 minutes ago
United StatesCareFusion 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 scanSpectra Medical Devices, Llc recalls Lidocaine HCl Injection USP
Lack of Assurance of SterilityGuardian Drug Co. Inc. recalls KIRKLAND Signature and 22 more products
Presence of foreign substance: small metallic particles in chewable tablets.Abiomed, Inc. recalls Automated Impella Controller
A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns.Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker
Incorrect inner package labeling.O&M Halyard Inc recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771
Nitrile Exam Glove failed to meet specifications chemical permeation performance.Philips Medical Systems Nederland B.V. recalls Azurion system and 1 more products
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service.Medtronic Neuromodulation recalls Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation and 1 more products
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.Bolton Medical Inc. recalls RelayPro Thoracic Stent-Graft System
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile.Abiomed, Inc. recalls Automated Impella Controller
Retrospective submission for following issues identified: 1.Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection and 6 more products
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including…A little guidance
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