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 1270112720 of 49,990 recalls

DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Revive Personal Products Company

Recalled Item: The Natural Dentist Healthy Breath Antiseptic Rinse Recalled by Revive...

The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril HCl/hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets 10 mg/12.5 mg 90...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2022· Acera Surgical Inc

Recalled Item: Restrata Recalled by Acera Surgical Inc Due to Misprinted expiration date on...

The Issue: Misprinted expiration date on the shelf-box

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Avanos Medical, Inc.

Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...

The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2022· Breas Medical, Inc.

Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...

The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2022· Varian Medical Systems Imaging Laboratory GmbH

Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...

The Issue: Software issue for treatment plan and image management application may...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2022· Advanced Accelerator Applications USA, Inc.

Recalled Item: NETSPOT (kit for the preparation of Ga 68 dotatate injection) 40 mcg...

The Issue: Subpotent Drug: low out-of-specification results for Vial 1 assay obtained...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· Olympus Corporation of the Americas

Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· ROi CPS LLC

Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...

The Issue: A drug kit component was recalled by its manufacturer due to the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2022· Hologic, Inc

Recalled Item: Panther Fusion GBS Assay Cartridges 96 Tests Recalled by Hologic, Inc Due to...

The Issue: Samples, run on a GBS Assay, that have analyte concentrations that are at or...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2022· Aurolife Pharma, LLC

Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Presence of...

The Issue: Presence of Foreign Substance: Complaint for pieces of glass discovered in a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2022· Intuitive Surgical, Inc.

Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...

The Issue: As a result of complaint data review, it identified tissue pushout events...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2022· Golden State Medical Supply Inc.

Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2022· Golden State Medical Supply Inc.

Recalled Item: Enalapril Maleate Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund