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 2814128160 of 50,591 recalls

DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Liberator Medical Supply Catheter Insertion Tray Recalled by Medline...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline All Purpose Instrument Tray Recalled by Medline Industries Inc Due...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Hip Replacement Recalled by Medline Industries Inc Due to Subpotent...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Catheter Insertion Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Circumcision Tray Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2017· Covidien LLC

Recalled Item: GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric...

The Issue: Reports of gastric or esophageal perforation occurring in procedures where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2017· Medtronic Neuromodulation

Recalled Item: Medtronic Ascenda(R) Intrathecal Catheter Recalled by Medtronic...

The Issue: There is a possibility that specific lots of catheters that have recently...

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

Class III — Low RiskOngoing
DrugSeptember 20, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: traces of Dapsone were found in the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Intuitive Surgical, Inc.

Recalled Item: daVinci X EndoWrist(R) Stapler 45 Recalled by Intuitive Surgical, Inc. Due...

The Issue: Specific da Vinci Xi EndoWrist Stapler 45 instruments are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2017· Exactech, Inc.

Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...

The Issue: There is a design incompatibility between certain sizes of the offset spine...

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

Class II — Potential Health HazardOngoing