Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,743 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,743 in last 12 months

Showing 4254142560 of 52,000 recalls

Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Vision Rt Inc

Recalled Item: AlignRT is a video-based three-dimensional (3D) surface imaging system which...

The Issue: Potential use error when the external Gate Controller is turned ON after...

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

Class II — Potential Health HazardOngoing
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Rio Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc. Due to Firm...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Whole Grain 5 Blend/Garden Vegetable 12/36 oz Product number 12410 Recalled...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Caviar Medley/Garden Vegetable 12/36 oz Product number 10610 Recalled by...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: White and Wild Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc....

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2014· InHarvest, Inc.

Recalled Item: Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden...

The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 10, 2014· Reckitt Benckiser LLC

Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...

The Issue: Defective container: A customer complaint revealed the presence of a...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...

The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· CSA Medical

Recalled Item: CSA Medical truFreeze System Recalled by CSA Medical Due to An increase in...

The Issue: An increase in complaint trending for a loss of audible sound associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Femoral Impactor ATTUNE INTUITION Impactor. The ATTUNE INTUITION Impactors...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· Arrow International Inc

Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...

The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue...

The Issue: Due to a complaint, it was determined that multiple lots of Licox catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: OSSEOTITE Tapered Certain Implant Rx Only Recalled by Biomet 3i, LLC Due to...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Breas Medical AB

Recalled Item: Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care Recalled...

The Issue: Unintended treatment termination could result from a keypad malfunction in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2014· Biomet 3i, LLC

Recalled Item: 3i T3 Non-Platform Switched Tapered Implant Rx Only Recalled by Biomet 3i,...

The Issue: Endosseous Dental Implants in contact with a residual machine fluid caused...

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

Class II — Potential Health HazardOngoing