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. 2,451 recalls have been distributed to Arkansas in the last 12 months.
Showing 25961–25980 of 28,355 recalls
Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Medtronic recently identified an issue with a subset of Consulta¿ CRT-P and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Multirate Infusor Devices. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Multiday lnfusor Recalled by Baxter Healthcare Corp. Due to Due...
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Schaedler K-V Agar with 5% Sheep Blood Recalled by Becton Dickinson &...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AOA Mini RPE Screw Assembly Recalled by Sybron Dental Specialties Due to The...
The Issue: The firm initiated the recall of AOA Mini RPE Screw Assembly, because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Campylobacter CSM Agar (Charcoal-Based Selective Medium) Recalled by...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375...
The Issue: Ortho Clinical Diagnostics is recalling CM/RT wear pads which are a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Brucella Laked Blood Agar with Kanamycin and Vancomycin (KV) Recalled by...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Device with Serosa Fastener and Accessories....
The Issue: Endogastric Solutions, Inc. has received a limited number of reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL BCYE Selective Agar with PAV Recalled by Becton Dickinson & Co. Due...
The Issue: Microbiological identification media may exhibit reduced levels of Vancomycin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.