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. 1,852 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,852 in last 12 months

Showing 2970129720 of 50,591 recalls

FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: HIPP Organic Comb Hungry Infant Milk Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· 3CS ORGANICS LLC

Recalled Item: Topfer Lactana Bio 1 Anfangsmilch Recalled by 3CS ORGANICS LLC Due to The...

The Issue: The product is not FDA approved and not all products are labeled in English.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2017· Z-Medica, LLC

Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...

The Issue: Packaging breach may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2017· Biosense Webster, Inc.

Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...

The Issue: Contraindication language updated in the Instructions For Use (IFU) to...

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

Class II — Potential Health HazardOngoing
DrugMay 17, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Presence of an impurity peak...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2017· X-Gen Pharmaceuticals Inc.

Recalled Item: Nystatin Topical Powder Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Presence of Foreign Substance: potential presence of plastic particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2017· Lupin Limited (Unit 1)

Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...

The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 16, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...

The Issue: Defective Delivery System: Elevated number of units with out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...

The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Beckman Coulter Inc

Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...

The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2017· Perkinelmer Life Sciences, Inc.

Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...

The Issue: Potential for electric shock in the case of a failure to install the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2017· Mesa Laboratories, Inc.

Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....

The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Philips Electronics North America Corporation

Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...

The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· Argon Medical Devices, Inc

Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...

The Issue: Argon Medical has received a complaint from one of their distributors of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2017· GE Medical Systems, LLC

Recalled Item: 1.5T Signa HDx Recalled by GE Medical Systems, LLC Due to Possible incorrect...

The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...

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

Class II — Potential Health HazardOngoing