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. 2,452 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,452 in last 12 months

Showing 3644136460 of 52,000 recalls

FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Southwest Salad Recalled by Dole Fresh Vegetables Inc Due to Dole is...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Leafy Romaine Salad Recalled by Dole Fresh Vegetables Inc Due to Dole is...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Caesar Kit Recalled by Dole Fresh Vegetables Inc Due to Dole is suspending...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Veggie Blend Recalled by Dole Fresh Vegetables Inc Due to Dole is suspending...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Colorful Coleslaw Display Recalled by Dole Fresh Vegetables Inc Due to Dole...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Southwest Salad Recalled by Dole Fresh Vegetables Inc Due to Dole is...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Coleslaw Recalled by Dole Fresh Vegetables Inc Due to Dole is suspending...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: All Natural Chopped Sesame Asian Family Kit Recalled by Dole Fresh...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 22, 2016· Dole Fresh Vegetables Inc

Recalled Item: Baby Spinach Recalled by Dole Fresh Vegetables Inc Due to Dole is suspending...

The Issue: Dole is suspending operations and withdrawing all marketed Dole and private...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Biomet France SARL

Recalled Item: Endobon-Xenograft Granules Recalled by Biomet France SARL Due to...

The Issue: Cytotoxicity tests were not passed at 36 months. Use of Endobon-Xenograft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...

The Issue: During a review of the packaging, it was determined that the seal integrity...

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

Class II — Potential Health HazardOngoing