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. 2,617 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,617 in last 12 months

Showing 1118111200 of 49,990 recalls

DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2022· Eclectic Institute Inc

Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...

The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System Recalled by Merit Medical Systems, Inc. Due to Biopsy...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2022· HERON THERAPEUTICS, INC.

Recalled Item: Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC....

The Issue: Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion 0.05% Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints received of defective container...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2022· Carwild Corporation

Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...

The Issue: Sterility with new cotton source not validated

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2022· Akorn, Inc

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Akorn, Inc Due to Defective...

The Issue: Defective Container: Product has incomplete induction seals.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· Randox Laboratories Ltd.

Recalled Item: The Randox Serology I Positive Control contains the following analytes...

The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· CAREFUSION

Recalled Item: BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site...

The Issue: Administration set, and extension set product labels list expiration year...

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

Class II — Potential Health HazardOngoing