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 1 minute ago
United StatesPercussionaire Corporation recalls Intrapulmonary Percussive Ventilation and 6 more products
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter…Shanghai United Imaging Healthcare Co., Ltd. recalls Computed Tomography X-ray System and 11 more products
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged…Merit Medical Systems, Inc. recalls Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam
Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile…Spectrum Medical SRL recalls Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High… and 1 more products
Due to blood-to-glycol leak in the heat exchanger.Philips North America recalls Ingenia Blue Seal SE and Blue Seal XE and 11 more products
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions).Medline Industries, LP recalls Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more products
Potential fire hazard involving the hand control pendant and associated wiring used with affected beds.ASP Global, LLC. recalls Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF and 63 more products
Due to incorrect expiration date on product manufactured between September 2016 to March 2023.Ajanta Pharma USA Inc recalls Ranolazine Extended-Release Tablets
Failed Dissolution Specifications: below specificationPar Health USA, LLC recalls Buprenorphine Hydrochloride
CrystallizationApotex Corp. recalls Paroxetine Extended-Release Tablets
Failed dissolution specifications.Aurobindo Pharma USA Inc recalls amazon
Discoloration: consumer complaints received for discolored tabletsTerSera Therapeutics LLC recalls Zoladex
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.Aurolab Trust recalls FOCUS PI Hypromellose 0.7% Formula
Lack of Assurance of SterilityAmneal Pharmaceuticals, LLC recalls Estradiol Gel
Defective Container; packets were found to be either empty or partially full.SV Labs Toronto Corporation recalls Benzoyl Peroxide Wash and 1 more products
Microbial contamination of topical product.Pacific Health Sciences Voluntarily Recalls One Lot of Babies' Magic Tea Brand Baby Sleep Gripe Water Dietary Supplement
Product contains undeclared ethanol, methanol, and isopropanol
Leader Formulas, LLC. Issues Voluntary Nationwide Recall of RAPTURE Preworkout Due to the Presence of 1,3-Dimethylamylamine (DMAA)
Product contains 1,3-Dimethylamylamine (DMAA)Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter
Software issue may cause a glucose result to be associated to the wrong patient
Greenwich Rx Issues Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels
Potential elevated endotoxin levelsBaxter Healthcare Corporation recalls Brand Name: VOLARA System Product Name: VOLARA
Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate.Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The…
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.Seaspine Orthopedics Corporation recalls SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head
The proximal thread depth of the spinal device is out of design specification.Philips Ultrasound, LLC recalls Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow…A little guidance
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