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. 2,480 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,480 in last 12 months

Showing 3208132100 of 52,000 recalls

Medical DeviceFebruary 3, 2017· Heartware

Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...

The Issue: Product recall of all HVAD Controllers currently on the market and to...

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

Class I — Serious Health HazardOngoing
DrugFebruary 2, 2017· Sandoz Inc

Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...

The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 2, 2017· Sage Products Inc

Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2017· Teva Pharmaceuticals USA

Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 2, 2017· B & H Foods Inc

Recalled Item: Ruth's Old Fashion Pimento Spread Recalled by B & H Foods Inc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 2, 2017· B & H Foods Inc

Recalled Item: Ruth's Original Pimento Spread 7oz () Recalled by B & H Foods Inc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 2, 2017· B & H Foods Inc

Recalled Item: Ruth's Lite Pimento Spread Recalled by B & H Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 2, 2017· B & H Foods Inc

Recalled Item: Ruth's Cream Cheese w/Pineapple-Pecans Recalled by B & H Foods Inc Due to...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 2, 2017· B & H Foods Inc

Recalled Item: Ruth's Jalapeno Pimento Spread Recalled by B & H Foods Inc Due to Potential...

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2017· Elcam Medical, Inc.

Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...

The Issue: The stopcock was found to have punctures.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Toshiba American Medical Systems Inc

Recalled Item: Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System...

The Issue: It was found that during a procedure the Peak Skin Dose (PSD) value...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Nidek Inc

Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...

The Issue: During treatment planning, the procedure was programmed with an unintended...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2017· Cook Inc.

Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...

The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...

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

Class II — Potential Health HazardOngoing