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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 21101–21120 of 28,355 recalls
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...
The Issue: There have been intermittent issues with Supercap POST (power on self-test)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...
The Issue: The item was recalled due to an increased user/patient risk of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...
The Issue: Damage to package seals potentially compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...
The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...
The Issue: Device non-conformity which may lead to an incorrect oscillometric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optional PS500 Power Supply Unit for the Evita V500 Ventilator Recalled by...
The Issue: The firm became aware of cases in which the battery run times of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.