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. 2,710 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,710 in last 12 months

Showing 901920 of 52,000 recalls

Medical DeviceOctober 31, 2025· Stryker Corporation

Recalled Item: NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination...

The Issue: Tape used to secure components within packaging contains latex, despite...

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

Class II — Potential Health HazardOngoing
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
FoodOctober 29, 2025· JFE FRANCHISING INC

Recalled Item: Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic Recalled by...

The Issue: Peaches provided by Moonlight Peaches potentially contaminated with Listeria.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 29, 2025· GBC Food Services, LLC

Recalled Item: Peach Salsa Recalled by GBC Food Services, LLC Due to Potential Listeria...

The Issue: Peaches provided by Moonlight Peaches potentially contaminated with Listeria.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2025· Medicrea International

Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...

The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens liquification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Copan Italia

Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...

The Issue: Treatment reagent functionality in respiratory specimens fluidification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Medtronic, Inc.

Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...

The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Night Formula) Recalled by Agebox Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2025· Agebox

Recalled Item: Agebox iKids-Growth (Day Formula) capsules Recalled by Agebox Due to...

The Issue: Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamoren

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2025· Moonlight Packing Corporation

Recalled Item: Sticker label (for Loose Bulk - peppermint peaches): 4401 Recalled by...

The Issue: Potential contamination with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2025· Moonlight Packing Corporation

Recalled Item: Peppermint Peach PROUCE OF U.S.A. Recalled by Moonlight Packing Corporation...

The Issue: Potential contamination with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund