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. 2,680 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,680 in last 12 months

Showing 17211740 of 50,591 recalls

Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: Epinephrine Injection Recalled by PFIZER INC Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· B BRAUN MEDICAL INC

Recalled Item: Lactated Ringer's Injection USP Recalled by B BRAUN MEDICAL INC Due to Lack...

The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....

The Issue: Potential that a component (air baffle) may be missing in some Nehalem...

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

Class II — Potential Health HazardOngoing
FoodJuly 31, 2025· Buffalo Rock Company Inc

Recalled Item: 7up Zero Sugar Tropical Soda Recalled by Buffalo Rock Company Inc Due to...

The Issue: Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing