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. 2,617 recalls have been distributed to Arkansas in the last 12 months.
Showing 10581–10600 of 28,355 recalls
Recalled Item: Covidien TA Auto Suture Vascular Loading Unit with DST Series Recalled by...
The Issue: May contain a damaged internal component which could impede staple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien TA Auto Suture Vascular Stapler with DST Series Technology Recalled...
The Issue: May contain a damaged internal component which could impede staple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT ES - Product Usage: intended for head Recalled by GE...
The Issue: A potential for protocol(s) with unintended patient orientation or scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT with Apex Edition CT System - Product Usage: intended for head...
The Issue: A potential for protocol(s) with unintended patient orientation or scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in...
The Issue: Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in...
The Issue: Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...
The Issue: There is the potential for the compounding system to not immediately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: There is a potential software error during programming.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...
The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HVAD Pump Implant Kits Recalled by Heartware, Inc. Due to Pumps...
The Issue: Pumps manufactured with impellers from a subset of lots from a single...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.