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. 2,666 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,666 in last 12 months

Showing 421440 of 49,990 recalls

DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...

The Issue: Presence of particulate matter - Glass like particles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
FoodDecember 17, 2025· ZIYAD BROTHERS IMPORTING

Recalled Item: Baraka French Style Puff Pastry 1lb and 1.5lbs sizes Recalled by ZIYAD...

The Issue: May contain partially hydrogenated oils

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 17, 2025· ZIYAD BROTHERS IMPORTING

Recalled Item: Baraka Gourmet Pastry Kunafe 6.7oz. Recalled by ZIYAD BROTHERS IMPORTING Due...

The Issue: May contain partially hydrogenated oils

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG) Recalled by...

The Issue: Lack of Assurance of Sterlity

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Dual Thread Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
DrugDecember 16, 2025· SpecGx, LLC

Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...

The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2025· SpecGx, LLC

Recalled Item: Oxycodone and Acetaminophen CII Tablets USP Recalled by SpecGx, LLC Due to...

The Issue: Failed Tablet/Capsule Specification: There is a potential for the imprint to...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing