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. 2,645 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,645 in last 12 months

Showing 38813900 of 13,434 recalls

DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets Recalled by...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Perrigo Fexofenadine Hydrochloride tablets Recalled by Perrigo Company PLC...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: allergyrelief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Health Mart Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: DG/health Aller.Ease Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2021· High Performance Formulas, L.L.C. (HPF, L.L.C.)

Recalled Item: Cholestene capsules Recalled by High Performance Formulas, L.L.C. (HPF,...

The Issue: Marketed Without an Approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidine Iodine Swabstick (1's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick Recalled by...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Cleansing Scrub Swabstick (1's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad Large Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Swabstick (3's) Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodine Prep Pad MEDIUM Recalled by Professional Disposables...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 23, 2021· Professional Disposables International, Inc

Recalled Item: PDI Povidone-Iodide Cleansing Scrub Swabstick (3's) Recalled by Professional...

The Issue: SubPotent: Out of Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 20, 2021· HIS ENTERPRISE INC

Recalled Item: Miss Slim Recalled by HIS ENTERPRISE INC Due to Marketed without ANDA/NDA...

The Issue: Marketed without ANDA/NDA approval

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2021· Teligent Pharma, Inc.

Recalled Item: Econazole Nitrate Cream 1% Recalled by Teligent Pharma, Inc. Due to Correct...

The Issue: Correct Labeled Product Mispack

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Tablet/Capsule Specification: Some tablets are shaved

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2021· Teligent Pharma, Inc.

Recalled Item: Triamcinolone Acetonide Ointment USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Correct Labeled Product Mispack

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2021· Alpha-Tek LLC

Recalled Item: ALPHA MALE+ Male Enhancer Recalled by Alpha-Tek LLC Due to Marketed Without...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2021· Johnson & Johnson Consumer, Inc.

Recalled Item: Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY Broad Spectrum SPF...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund