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 1340113420 of 49,990 recalls

DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: CVS Health Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: equate Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Rugby Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Wal-Fex D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddys Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Rite Aid Pharmacy Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Leader Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Kroger Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 4, 2022· BALT USA, LLC

Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...

The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2022· Smith & Nephew, Inc.

Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....

The Issue: The affected screwdrivers are out of specification and may not mate with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2022· Philips North America Llc

Recalled Item: eCareManager version 4.2.1 Recalled by Philips North America Llc Due to...

The Issue: eCareManager (eCM) Sentry Score software not approved for use

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2022· Immuno-Mycologics, Inc

Recalled Item: CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY Recalled by Immuno-Mycologics, Inc...

The Issue: The firm found immunoassay products used to detect cryptococcal antigen in...

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

Class II — Potential Health HazardOngoing
DrugDecember 31, 2021· Rubicon Research Private Limited

Recalled Item: Metoprolol Tartrate Tablets Recalled by Rubicon Research Private Limited Due...

The Issue: Complaint received of foreign matter (metal) embedded in tablet.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation/RayPlan- designed for treatment planning and analysis of...

The Issue: If a new primary image set is selected while the cine loop is running, the...

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

Class II — Potential Health HazardOngoing
DrugDecember 29, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Pioglitazone Tablets USP Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Superpotent and Failed Tablet/Capsule Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 29, 2021· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes Recalled by MEDLINE...

The Issue: Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2021· Stryker Leibinger GmbH & Co. KG

Recalled Item: MEDPOR Titan OFW - MTB - Right - 1.0mm Recalled by Stryker Leibinger GmbH &...

The Issue: Inside the packaging of one reported item a non-conforming product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion Pumps Recalled by Baxter Healthcare Corporation...

The Issue: There is the potential for reduced or non-delivery of medication, in some...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: There is the potential for reduced or non-delivery of medication, in some...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 28, 2021· Hobbs Medical, Inc.

Recalled Item: Bronchial Microbiology Brush Recalled by Hobbs Medical, Inc. Due to The...

The Issue: The labeling for the Microbiology Brush identifies the device as a Bronchial...

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

Class II — Potential Health HazardOngoing