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 7 minutes ago
United StatesBecton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date.Orthofix U.S. LLC recalls Virata Preassembled Polyaxial Screw
Polyaxial screws do not meet performance standards.Miach Orthopaedics recalls BEAR Implant
The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk stock only.NeuroLogica Corporation recalls GM85 Digital Mobile X-ray imaging System
The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.Sonesta Medical AB recalls Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software…
Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.Abbott Laboratories recalls Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number…
Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.Olympus Corporation of the Americas recalls Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use… and 1 more products
Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.Abbott Medical recalls Eterna SCS IPG and 1 more products
There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS)…Accriva Diagnostics, Inc. recalls VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The…
Due to an device without a premarket clearance being incorrectly package and distributed.Siemens Healthcare Diagnostics, Inc. recalls IMMULITE 2000 Oak Mix Specific Allergen and 2 more products
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge.Philips Respironics, Inc. recalls SimplyGo Mini
Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output…Medline Industries, LP recalls Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits and 9 more products
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing.Cerenovus Inc recalls CEREPAK Detachable Coil System
Detachable coils system may fail to detach, which could result in hemorrhagic and ischemic stroke, procedural delays, or the need for additional surgical intervention.Covidien, 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.FreshRealm recalls Loaded Veggie Grain Bowl
Potential contamination with Listeria monocytogenesSingh Trading Inc. DBA Roshni Foods recalls Roshni Cinnamon Powder
Product may contain elevated levels of lead and chromium.A little guidance
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