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. 1,034 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,034 in last 12 months

Showing 21321–21340 of 50,591 recalls

Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Komuro Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle133 Plus Tissue Expander With/Without Suture Tabs Recalled by...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 150 Full Height and Short Height Implants Recalled by Allergan PLC...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2019· Wilson-Cook Medical Inc.

Recalled Item: Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc. Due to...

The Issue: Potential for Hemospray device to be unable to spray powder due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2019· Allergan PLC

Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...

The Issue: The action was initiated following notification by the U.S. FDA of their...

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

Class I — Serious Health HazardOngoing
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Great Value Mild Taco Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Ingredients Recalled by CH Guenther & Sons, Inc Due to Potential...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Original Chili Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: HEB Taco Seasoning Mix 25% Less Sodium Net Wt. 1.25 OZ Recalled by CH...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Winco Foods Recalled by CH Guenther & Sons, Inc Due to Potential Salmonella...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2019· New Standard Device Inc

Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...

The Issue: The threads on posts stripping out when tensioned during application process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...

The Issue: An error can occur when performing a biopsy using the InSpect function. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing