Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 3068130700 of 50,591 recalls

Medical DeviceApril 3, 2017· Natus Medical Incorporated

Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...

The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRONE Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Cell Distributors

Recalled Item: Tears (Carboxymethylcellulose Sodium Solution) 0.5% Recalled by Cell...

The Issue: Labeling: Not elsewhere classified; product labeling lacks a NDC number, net...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 31, 2017· ConAgra Foods Inc

Recalled Item: Premium Hunt's Chili Kit Recalled by ConAgra Foods Inc Due to Potential...

The Issue: Potential Salmonella contamination of spice packet within chili kits.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 31, 2017· Pinnacle Foods, LLC

Recalled Item: Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores...

The Issue: Glass fragments were found in Great Value Bread and Butter Chips.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 31, 2017· Reser's Fine Foods, Inc.

Recalled Item: Reser's Fine Foods Recalled by Reser's Fine Foods, Inc. Due to Undeclared Milk

The Issue: Product contains undeclared milk and soy.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 31, 2017· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi EndoWrist Suction Irrigator Recalled by Intuitive Surgical, Inc....

The Issue: Intuitive Surgical has become aware that in specific scenarios with system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2017· Oscor, Inc.

Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...

The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2017· C.R. Bard, Inc.

Recalled Item: Arctic Sun 5000 Temperature Management System Recalled by C.R. Bard, Inc....

The Issue: Potential failure of the Arctic Sun 5000 Temperature Management System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2017· Oscor, Inc.

Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...

The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing