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 12 minutes ago
United States
Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter
Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steel
Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter
Presence of particulate matter identified as celluloseKarl Storz Endoscopy recalls HOPKINS Telescope 30¿
Due to incorrect inside packaging label for eyepiece.Noxbox LTD recalls NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.
Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Revised C-Reactive Protein
The potential for falsely elevated results.HeartSine Technologies Ltd recalls HeartSine samaritan PAD
Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.Tandem Diabetes Care, Inc. recalls Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application
A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application with…Beckman Coulter Mishima K.K. recalls Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480…
Certain AU480 chemistry analyzers, with Windows 10 IoT Enterprise 2021 LTSC PCs, may output the message System Stopped By Fatal Error: DBConnectionError AlarmDB when…Olympus Corporation of the Americas recalls Olympus Tripp-Lite P580-025 25ft DisplayPort Cable
While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable.Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw
Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used…Heraeus Medical GmbH (Dental Division) recalls PALACOS R pro 40 and 3 more products
Potential for monomer liquid leakage.Bard Peripheral Vascular Inc recalls EnCor EnCompass Breast Biopsy and Tissue Removal System Console
Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) Pressure…Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code…
Due to incorrect label/product dimensions.Olympus Corporation of the Americas recalls Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A. and 1 more products
There are identified discrepancies between the sterilization parameters listed in the Instructions for Use and the sterilization parameters listed in the Japanese…Illumina, Inc. recalls NovaSeq 6000Dx including DRAGEN Server
Retrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro diagnostic assays has…Draeger, Inc. recalls VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable…
Potential cracks in the hose, which could lead to leakage or the hose falling off.Alere San Diego, Inc. recalls McKesson CONSULT hCG Urine Cassette and 3 more products
hCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result.Philips North America Llc recalls Philips Medical Systems Technologies Ltd. Spectral CT 7500
The Bolus tracking scan application may crash with a system error message.Penumbra Inc. recalls Brand Name: Penumbra System
Due to manufacturing issues reperfusion catheters may fracture.American Nitrile Operations Llc recalls Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number: 72-RM50601 and 2 more products
Gloves may exhibit defects such as tears, missing fingers, and debris.Custom Interventional Pain Management, LLC recalls Brand Name: Ferndale Laboratories
Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.Volcano Corp recalls Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v
Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.American Contract Systems Inc recalls Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary… and 2 more products
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the…A little guidance
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