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 1601–1620 of 49,990 recalls
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringers's Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EverPatch+ Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have...
The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICEfx Cryoablation System Recalled by Boston Scientific Corporation Due to...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...
The Issue: Certain desiccant tube subassemblies were built with end caps that were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peanut rounds 2.25 oz and 3 oz Recalled by Anderson Candy Company, LLC Due...
The Issue: Undeclared soy allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging...
The Issue: Product may be contaminated with Cesium-137 (Cs-137)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...
The Issue: Potential for activation of an abnormal alarm pause.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...
The Issue: Potential for barb non-engagement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.