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 2866128680 of 50,591 recalls

FoodJuly 19, 2017· TRULY GOOD FOODS

Recalled Item: Pumpkin Seeds Recalled by TRULY GOOD FOODS Due to Undeclared Allergen

The Issue: Undeclared allergen Tree Nuts: Blackened Seasoned Pumpkin Seeds mixed up...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2017· Teleflex Medical

Recalled Item: Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with...

The Issue: For some of the recalled products, the security of the connection between...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 6000 Modular Series system Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 MODULAR Series System - c501 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Corporation...

The Issue: A warning is being added to the cobas¿ 6000 analyzer and the cobas¿ 8000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Medline Industries Inc

Recalled Item: Sterile Elastic Esmark Bandage Recalled by Medline Industries Inc Due to...

The Issue: Product did not undergo correct sterilization procedures and may potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2017· Vyaire Medical

Recalled Item: AirLife(TM) Reduced Heparin ARTERIAL BLOOD SAMPLER Recalled by Vyaire...

The Issue: Lot #0001047501 of the 9025RHTR ABG sampling kits have been manufactured...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2017· BESTHERBS COFFEE LLC

Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 17, 2017· NatureBox, Inc.

Recalled Item: NatureBox Sticks 'n Stones Recalled by NatureBox, Inc. Due to Firm received...

The Issue: Firm received notification that a consumer found a peanut in NatureBox...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 17, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Product Usage: is a software system designed for treatment...

The Issue: For the proton QA preparation module in RayStation 6 (including SP1 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100i Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 300 Intra-Aortic Balloon Pump. It supports the heart's left Recalled by...

The Issue: False blood back detection alarm and the ingress of fluids into the IABP...

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

Class I — Serious Health HazardOngoing
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg)...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund