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. 2,400 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,400 in last 12 months

Showing 4866148680 of 52,000 recalls

FoodMarch 15, 2013· Grippo Potato Chip Co., Inc.

Recalled Item: Grippo's Salt & Vinegar FLAVORED POTATO CHIPS Recalled by Grippo Potato Chip...

The Issue: During an inspection by the Ohio Department of Agriculture, the firm was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2013· Grippo Potato Chip Co., Inc.

Recalled Item: Grippo's CHEDDAR CHEESE WITH A TOUCH OF JALAPENO natural & Recalled by...

The Issue: During an inspection by the Ohio Department of Agriculture, the firm was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2013· Grippo Potato Chip Co., Inc.

Recalled Item: Grippo's Sweet BERMUDA ONION FLAVORED POTATO CHIPS Recalled by Grippo Potato...

The Issue: During an inspection by the Ohio Department of Agriculture, the firm was...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2013· Grippo Potato Chip Co., Inc.

Recalled Item: Grippo's HOT DILL PICKLE Artificially Flavored Potato Chips Recalled by...

The Issue: During an inspection by the Ohio Department of Agriculture, the firm was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 15, 2013· MCKESSON TECHNOLOGIES INC.

Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...

The Issue: There was an occurrence where the patient case data did not match the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Acist Medical Systems

Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...

The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· AGFA Corp.

Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...

The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...

The Issue: Non-Sterility; mold contamination

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 14, 2013· Med Prep Consulting, Inc.

Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for mold contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...

The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 14, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...

The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Synvasive Technology Inc

Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...

The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...

The Issue: Two unsealed pouches were found at an Edwards' distribution location in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2013· Elekta, Inc.

Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...

The Issue: The Column rotation can accidentally be moved to a different position which...

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

Class II — Potential Health HazardOngoing
FoodMarch 13, 2013· Daesang America Inc

Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...

The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...

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

Class I — Serious Health HazardOngoing
Refund