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. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 7021–7040 of 28,355 recalls
Recalled Item: Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator...
The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...
The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity central lab Recalled by Roche Diagnostics Operations, Inc....
The Issue: A complaint investigation revealed that an incorrect behavior relating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal ORGAN RECOVERY PACK PGYBK Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedBank System - Product Label/labeling pending Recalled by...
The Issue: Due to customer complaints related to the MedBank software which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Steam Test Pack (20 Tests and 5 controls) Item Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...
The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...
The Issue: There is an increased chance that the tests from affected lots may give...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.