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. 2,553 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,553 in last 12 months

Showing 1722117240 of 28,641 recalls

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 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
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 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 18, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...

The Issue: Increased amount of residual blood present on the top of stopper well after...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2017· MicroPort Orthopedics Inc.

Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...

The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2017· Encore Medical, Lp

Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...

The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2017· HILL-ROM MANUFACTURING, INC.

Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...

The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2017· Encore Medical, Lp

Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...

The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2017· C.R. Bard, Inc.

Recalled Item: HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box...

The Issue: Several instances of a catheter caught in the sterile barrier seal and in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2017· C.R. Bard, Inc.

Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...

The Issue: Several instances of a catheter caught in the sterile barrier seal and in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2017· C.R. Bard, Inc.

Recalled Item: Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box...

The Issue: Several instances of a catheter caught in the sterile barrier seal and in...

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

Class II — Potential Health HazardOngoing