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. 2,661 recalls have been distributed to Arkansas in the last 12 months.
Showing 2961–2980 of 28,355 recalls
Recalled Item: MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing...
The Issue: There is a potential for pinholes in the applicator pouch film which creates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z-800 Infusion System Recalled by Zyno Medical LLC Due to There is a defect...
The Issue: There is a defect in the air-in-line software algorithm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m HPV AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity m STI AMP Kit Recalled by Abbott Molecular, Inc. Due to...
The Issue: Abbott has identified an increase of incidences regarding Error Code (EC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Life2000 Ventilation System Recalled by Baxter Healthcare...
The Issue: The Life2000 ventilator may fail to initiate the Low Gas Pressure alarm if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution with software versions: 4.20 Recalled by...
The Issue: Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access...
The Issue: Exposure of the UroPass product to Ultraviolet ( UV ) Radiation can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Infusion Pump. Product Number: 8637-20 Recalled by Medtronic...
The Issue: Potential for error and inability to interrogate pump due to data corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK Universal Handle Recalled by Waldemar Link GmbH & Co. KG (Corp. Hq.)...
The Issue: Some lots of the LINK Universal Handle, with quick coupling, Stainless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCast Covered Stent Recalled by Atrium Medical Corporation Due to There is...
The Issue: There is an error in the Unique Device Identifier (UDI) printed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor...
The Issue: Safety glasses with Rx indoor universal lenses fail to meet high impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment Recalled...
The Issue: X-ray R/F system software with certain versions of the control board may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FLUOROspeed is intended to be used as a universal Recalled by SHIMADZU...
The Issue: X-ray R/F system software with certain versions of the control board may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias unity Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due...
The Issue: If digital angiography system is used with a specific catheterization table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific myLUX Patient Application for an Apple Mobile device...
The Issue: Patients using the Model 2939 myLUX Patient Application on their Apple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise Imaging XERO Viewer- software application used for and Recalled...
The Issue: Software defect, when an image has non-square pixel spacing, the /localizer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin Antibody II Recalled by Beckman Coulter, Inc. Due to...
The Issue: IFUs for the device incorrectly states the biotin interference was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...
The Issue: Boston Scientific has received reports indicating the grid mark overlay on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...
The Issue: Boston Scientific has received reports indicating the grid mark overlay on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...
The Issue: Boston Scientific has received reports indicating the grid mark overlay on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.