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. 2,598 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,598 in last 12 months

Showing 1350113520 of 49,990 recalls

DrugDecember 21, 2021· Ascend Laboratories, LLC

Recalled Item: Cefixime Capsules Recalled by Ascend Laboratories, LLC Due to Failed...

The Issue: Failed impurities/degradation specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant Recalled by Medtronic Vascular, Inc. Due to Stent Graft Systems...

The Issue: Stent Graft Systems built with specific batches of taper tip assemblies have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 20, 2021· American Health Packaging

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by American Health...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2021· Professional Complementary Health Formulas, LLC

Recalled Item: Inositol packaged in white plastic bottle with and Recalled by Professional...

The Issue: Product recalled due to undeclared niacin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2021· Professional Complementary Health Formulas, LLC

Recalled Item: Vitamin B Complex packaged in white plastic bottle labeled in part Recalled...

The Issue: Product recalled due to undeclared niacin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 20, 2021· DREAM POPS

Recalled Item: 100% Plant-Based Dream Pops Vanilla Sky Bites Recalled by DREAM POPS Due to...

The Issue: Undeclared allergen; milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 20, 2021· DREAM POPS

Recalled Item: 100% Plant-Based Dream Pops Berry Dreams Bites Recalled by DREAM POPS Due to...

The Issue: Undeclared allergen; milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 20, 2021· DREAM POPS

Recalled Item: 100% Plant-Based Dream Pops Birthday Cake Bites Recalled by DREAM POPS Due...

The Issue: Undeclared allergen; milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 20, 2021· DREAM POPS

Recalled Item: 100% Plant-Based Dream Pops Cookie Dough Bites Recalled by DREAM POPS Due to...

The Issue: Undeclared allergen; milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 20, 2021· Vyaire Medical

Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to Potential...

The Issue: Potential cessation in ventilation can occur under specific conditions.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2021· Canon Medical System, USA, INC.

Recalled Item: Flat Panel Detector Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Abnormal images such as horizontal stripes may be displayed and recovery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Nobel Biocare Usa Llc

Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...

The Issue: Due to 16 complaints related to drivers not engaging in implants. According...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Covidien Llc

Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...

The Issue: The firm has received six (6) complaint reports from customers indicating...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 16, 2021· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

The Issue: Subpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2021· Draeger Medical, Inc.

Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...

The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 15, 2021· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Clobetasol Propionate Ointment USP Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of R. Pickettii...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20545 Vitale Silver calcium Alginate Dressings 4x5 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20522 Vitale Silver calcium Alginate Dressings 2x2 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing