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. 2,494 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,494 in last 12 months

Showing 2398124000 of 50,591 recalls

Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Zimmer Biomet, Inc.

Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...

The Issue: Screw is missing from the package

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· Cardinal Health 200, LLC

Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...

The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2018· COVIDIEN LLC

Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...

The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2018· Horiba Instruments Incorporated

Recalled Item: Clinical Chemistry Recalled by Horiba Instruments Incorporated Due to...

The Issue: Potential for chemical analyzer to report abnormal results due to an...

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

Class II — Potential Health HazardOngoing
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Westminster Pharmaceuticals Llc

Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...

The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Akorn, Inc.

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Akorn, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 29, 2018· Sciegen Pharmaceuticals Inc

Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2018· Feast Mode Blending & Filling

Recalled Item: Feast Mode Flavors Garlic Beer Seasoning Recalled by Feast Mode Blending &...

The Issue: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Levetiracetam in 0.54 % Sodium Chloride Injection 1 Recalled by Dr. Reddy's...

The Issue: Labeling: Label Error on Declared Strength; the pre-printed text on the...

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

Class I — Serious Health HazardOngoing
Refund