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. 1,076 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,076 in last 12 months

Showing 15821–15840 of 52,000 recalls

Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Accora Inc

Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...

The Issue: The firm has identified a potential for the backrest to become detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Murata Vios, Inc.

Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...

The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...

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

Class II — Potential Health HazardOngoing
DrugJune 21, 2021· Prairie Wolf Spirits

Recalled Item: Prairie Wolf Distillery Alcohol Antiseptic 80% Recalled by Prairie Wolf...

The Issue: Hand sanitizer packaged in bottles that resemble beverage containers.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 18, 2021· Teva Pharmaceuticals USA

Recalled Item: Topotecan Injection 4 mg/4mL (1 mg/mL) Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Particulate Matter: Complaint received of a glass particle...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 18, 2021· Remel Inc

Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...

The Issue: Out of Specification

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2021· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....

The Issue: It has been identified that ventilators equipped with High Flow Therapy...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2021· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...

The Issue: It has been identified that ventilators equipped with High Flow Therapy...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2021· WOM World of Medicine AG

Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...

The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...

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

Class II — Potential Health HazardOngoing
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by India Curry Recalled by Cuisine Solutions Due to...

The Issue: Undeclared egg and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by America Roasted Potato Recalled by Cuisine Solutions...

The Issue: Undeclared egg and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by Mexico Roasted Poblanos Recalled by Cuisine Solutions...

The Issue: Undeclared egg and milk

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by Japan Portobello Recalled by Cuisine Solutions Due to...

The Issue: Undeclared egg and milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 17, 2021· Gentherm Medical, LLC

Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...

The Issue: There is a potential risk of device contamination and patient infection...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2021· Medicalplastic S.R.L.

Recalled Item: Ilizarov Wire Tensioner Recalled by Medicalplastic S.R.L. Due to...

The Issue: Medicalplastic s.r.l. is conducting a voluntary field action to remove a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2021· Cardinal Health 200, LLC

Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...

The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...

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

Class I — Serious Health HazardOngoing
DrugJune 16, 2021· Spirit Pharmaceuticals

Recalled Item: Acetaminophen 325 mg tablets Recalled by Spirit Pharmaceuticals Due to cGMP...

The Issue: cGMP deviations: Discolored acetaminophen

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 14, 2021· Arthrex, Inc.

Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...

The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...

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

Class II — Potential Health HazardOngoing