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. 1,856 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,856 in last 12 months

Showing 3098131000 of 49,990 recalls

Medical DeviceJanuary 20, 2017· Metrex Research, LLC.

Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...

The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Atrium Medical Corporation

Recalled Item: Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008 Recalled by...

The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Integra LifeSciences Corp.

Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....

The Issue: Posterior tibial fractures have been reported.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· Atrium Medical Corporation

Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...

The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2017· GE Healthcare, LLC

Recalled Item: Discovery MR450 The systems are whole body magnetic resonance scanners...

The Issue: Potential safety issue with the patient bore heating on the Discovery MR450...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Mirtazapine Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2017· LEO PHARMA INC

Recalled Item: Calcipotriene Cream 0.0005% Recalled by LEO PHARMA INC Due to Undeclared...

The Issue: Incorrect/Undeclared excipients: inadvertent omission of a drug excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: glipiZIDE Extended-Release Tablets Recalled by Mylan Pharmaceuticals Inc....

The Issue: Presence of Foreign Tablets/Capsules; bottles of Glipizide 5 mg tablets may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Metoclopramide Oral Solution Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Methadone Hydrochloride Oral Concentrate Recalled by VistaPharm, Inc. Due to...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to CGMP...

The Issue: CGMP Deviations: Purified water used to manufacture the drug products may...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 18, 2017· D. F. Stauffer Biscuit Co, Inc.

Recalled Item: FRONT: Stauffer's Animal Crackers Original Recalled by D. F. Stauffer...

The Issue: D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling one specific best...

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

Class I — Serious Health HazardOngoing
Refund