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 3686136880 of 52,000 recalls

Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Cashew Cow Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared sub-ingredient soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Chocolate Marshmallows Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy and milk (butter declared).

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...

The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· Zingerman's Candy Manufactory

Recalled Item: Zzang! Holiday 4 pack Candy Bars Recalled by Zingerman's Candy Manufactory...

The Issue: Product recalled due to undeclared soy; and undeclared allergen milk (cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2015· This Bar Saves Lives

Recalled Item: This Kid Saves Lives Chocolate Chip #10858497004097 UPC# 858497004090...

The Issue: This Bar Saves Lives is recalling This Kid Saves Lives Chocolate Chip...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2015· GE Medical Systems, LLC

Recalled Item: Mavig Monitor Suspension System Recalled by GE Medical Systems, LLC Due to...

The Issue: GE Healthcare has recently become aware of a reported incident in which a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· C.R. Bard, Inc.

Recalled Item: BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter Recalled by C.R. Bard,...

The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· Arkray Factory USA, Inc.

Recalled Item: arkray SPOTCHEM II Basic Panel - 1 Reagent test strips Recalled by Arkray...

The Issue: One lot each of SPOTCHEM II Basic PANEL-1 Reagent Test Strip and SPOTCHEM II...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2015· Elekta, Inc.

Recalled Item: Oncentra External Beam - VMAT - Radiation therapy planning system Recalled...

The Issue: When using the option "Tumor Overlap Fraction" in VMAT planning it has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· Stryker Spine

Recalled Item: Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine...

The Issue: Reported jamming of the impaction handle when assembled to the Inserter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· Arkray Factory USA, Inc.

Recalled Item: arkray SPOTCHEM II Glucose Reagent test strips Recalled by Arkray Factory...

The Issue: One lot each of SPOTCHEM II Basic PANEL-1 Reagent Test Strip and SPOTCHEM II...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2015· C.R. Bard, Inc.

Recalled Item: BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary...

The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· C.R. Bard, Inc.

Recalled Item: BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter Recalled by C.R....

The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· EndoChoice, Inc.

Recalled Item: Fuse 1C Colonoscope Recalled by EndoChoice, Inc. Due to The bending section...

The Issue: The bending section of the device may partially separate from the insertion...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· NeoCoil, LLC

Recalled Item: NeoCoil 3.0T GEM Flex Coil. The 3.0T GEM Flex coil Recalled by NeoCoil, LLC...

The Issue: Potential for higher than specified surface temperatures. Use of 3.0T GEM...

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2015· National Vitamin Co Inc

Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...

The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...

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

Class III — Low RiskOngoing
Refund