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 6 minutes ago
United StatesCovidien, LP recalls Covidien Signia" Small Diameter Curved Tip Intelligent Reload and 1 more products
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for…Medline Industries, LP recalls Medline Renewal LigaSure Exact and 10 more products
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases…GE Healthcare Finland Oy recalls Carescape B450 and 4 more products
Potential loss of monitoring on affected monitors when powered by certain batteries.Techno-Path Manufacturing LTD. recalls Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive… and 1 more products
Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.Philips Medical Systems DMC GmbH recalls ProxiDiagnost N90 and 5 more products
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e.Olympus Corporation of the Americas recalls Brand Name: Lithotriptor
The device may either fail to start up, or the transducer may start briefly and then stop, accompanied by an error light on the generator.Applied Medical Technology Inc recalls Applied Medical Technology and 4 more products
The nasal feeding tube may be occludedMedtronic Perfusion Systems recalls Affinity NT Oxygenator
Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas transfer rates that did not meet performance requirements.Integra LifeSciences Corp. (NeuroSciences) recalls TruDi¿ Navigation System
It was determined that when the navigation system is configured with specific revision combinations of the Multi Instrument Adapter together with the Patient Tracker…Beckman Coulter Inc. recalls SYNCHRON Systems Direct LDL Cholesterol
Beckman Coulter has identified that there is an increased probability Synchron Systems Direct LDL Cholesterol (LDLD REF 969706) reagent lot M404166 may generate false…Tandem Diabetes Care, Inc. recalls Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated…
Insulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions.Elekta, Inc. recalls Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage Stereotactic…
Due to increased risk that paint flakes from the engravings may separate from the device and there is the possibility that the flake may inadvertently enter the woundSpacelabs Healthcare, Ltd. recalls Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software…
Due to two distinct issues: 1.Total Joint Orthopedics, Inc. recalls Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic BiPolar Head
Potential packaging issue that could compromise the sterile barrier.Beckman Coulter, Inc. recalls Beckman Coulter UniCel DxI 600 and 1 more products
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an…Zimmer, Inc. recalls Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene and 1 more products
Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle.OSSTEM Implant Co., Ltd. recalls Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS. and 2 more products
Osstem Implant Co.B-K Medical A/S recalls 1202 Flex Focus Ultrasound System and 5 more products
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement…Integra LifeSciences Corp. (NeuroSciences) recalls CODMAN Disposable Perforator 11mm. Cranial Perforator. and 1 more products
Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.Mozarc Medical US LLC recalls MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC… and 5 more products
A potential issue with the seal integrity of header bag packaging.Prismatik Dentalcraft, Inc. recalls Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i"…
Incorrect titanium screw, packaged with dental implant.Zydus Pharmaceuticals (USA) Inc recalls clomiPRAMINE Hydrochloride and 2 more products
cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable…Aero Healthcare recalls Acetaminophen 500mg Caffeine 65mg caplets
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