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. 2,662 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,662 in last 12 months

Showing 13411360 of 13,434 recalls

DrugNovember 9, 2023· Family Medical Supply Inc

Recalled Item: Oxygen Recalled by Family Medical Supply Inc Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2023· SUGARMDS LLC

Recalled Item: Dr. Ergin's SugarMD Recalled by SUGARMDS LLC Due to MARKETED WITHOUT AN...

The Issue: MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin 25mg Capsules Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2023· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: VITRAKVI (larotractenib) oral solution Recalled by Bayer Healthcare...

The Issue: Microbial Contamination of Non-Sterile Products: microbial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 6, 2023· Taro Pharmaceuticals Inc.

Recalled Item: Hydrocortisone 1% and Acetic Acid 2% Otic Solution USP Recalled by Taro...

The Issue: Failed Impurities/Degradation Specifications:Out-of-Specification result for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2023· Padagis US LLC

Recalled Item: Trospium Chloride Extended-Release Capsules Recalled by Padagis US LLC Due...

The Issue: Failed Tablets/Capsules specifications; missing/broken/extra tablets within...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2023· Apotex Corp.

Recalled Item: Paroxetine Hydrochloride Tablets USP Recalled by Apotex Corp. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications-Out of specification (OOS)...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Lisinopril Tablets USP 20 mg Recalled by NCS Healthcare of Kentucky Inc Due...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund