Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,462 recalls have been distributed to Arkansas in the last 12 months.
Showing 24701–24720 of 28,355 recalls
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pega Medical Inc. Recalled by Pega Medical Inc. Due to The Male Components...
The Issue: The Male Components in this lot are made of material with lower strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMP X-alt Acetabular Liner This acetabular liner is intended for Recalled by...
The Issue: Packaging error -- two different types and sizes of acetabular liners used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product...
The Issue: Baxter Healthcare Corporation has issued an Urgent Device Correction for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee Angiographic x-ray systems. Recalled by Siemens Medical Solutions...
The Issue: An inappropriate cable connection was assembled for certain Artis zee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Recalled by...
The Issue: The battery capacity of the optional PS500 Power Supply Unit of the Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...
The Issue: Incorrect master label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...
The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...
The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F18Nre Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NRe High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu AlB & RSV Direct Assay Kits Recalled by Focus Diagnostics Inc...
The Issue: Focus Diagnostics initiated the recall of the certain Simplexa Flu AlB & RSV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator used Model numbers: M3535A...
The Issue: HeartStart MRx Defibrillator Monitor therapy connection could experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F200NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux F160NR High Flux Dialyzers Recalled by Fresenius Medical Care...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.