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 1314113160 of 49,990 recalls

Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 SYPH T PACK Syphilis Total & RPR Reagent Pack Recalled by...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Syphilis Total & RPR Calibrator Set CAL Recalled by Bio-Rad...

The Issue: Due to current concerns related to COVID-19 vaccine interference with the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2022· Tsm Brands LLC

Recalled Item: Luxury 70% Isopropyl Alcohol Recalled by Tsm Brands LLC Due to Undeclared Ethyl

The Issue: Labeling - product contains undeclared ethyl alcohol

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2022· Tsm Brands LLC

Recalled Item: 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen Recalled by Tsm...

The Issue: Labeling - product contains undeclared ethyl alcohol

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2022· RISING PHARMACEUTICALS

Recalled Item: Methylphenidate Hydrochloride Chewable Tablets Recalled by RISING...

The Issue: Failed Tablet Specifications: Recall of this drug product was voluntarily...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Chlorthalidone Tablets USP 25 mg Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: Foreign Matter identified as stainless steel microscopic wear particles...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2022· Teligent Pharma, Inc.

Recalled Item: Erythromycin Topical Gel USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Lot not meeting specification...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 7, 2022· Mohammad Mayha

Recalled Item: Jaguar Power Honey packaged in a gold paper box with black writing Recalled...

The Issue: Contains hidden drug ingredient

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 7, 2022· Mohammad Mayha

Recalled Item: Helmi Honey VIP packaged in a gold paper box with black writing Recalled by...

The Issue: Contains hidden drug ingredient

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 7, 2022· Philips North America, LLC

Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...

The Issue: Update to instructions for use regarding the cleaning and disinfection...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2022· Brius Technologies Inc.

Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...

The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...

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

Class II — Potential Health HazardOngoing
DrugFebruary 4, 2022· Professional Disposables International, Inc.

Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab Recalled by...

The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2022· Professional Disposables International, Inc.

Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick...

The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2022· Professional Disposables International, Inc.

Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick...

The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2022· CooperSurgical, Inc

Recalled Item: PARAGARD T380A (intrauterine copper contraceptive) Recalled by...

The Issue: Non-sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 4, 2022· Junp Hydration LLC

Recalled Item: MegMan Performance Booster Recalled by Junp Hydration LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2022· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...

The Issue: There is a potential for AED pads to experience gel separation from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2022· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...

The Issue: There is a potential for AED pads to experience gel separation from the...

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

Class II — Potential Health HazardOngoing