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 15321–15340 of 52,000 recalls

Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: Stretch Leveller Model Number: 3156200 - The combination of this Recalled by...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: FlexoStretch Model Number: 3156057 - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: OctoStretch with Stretch Leveller - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Recalled...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
FoodAugust 11, 2021· RMH Foods

Recalled Item: Gordon Choice Deli Style Tuna Salad Recalled by RMH Foods Due to Undeclared...

The Issue: Undeclared wheat and tuna

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 11, 2021· Ebay Seller - John Nguyen

Recalled Item: Hydro Pinapple Burn Max Health Thach Dua Recalled by Ebay Seller - John...

The Issue: Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Non-Sterility: firm's third party lab confirmed microbial contamination.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: V1500HP OUTLOOK PUMP SET 118-single-use for use with the Outlook Recalled by...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Add-On Set-single use Recalled by B. Braun Medical, Inc. Due to...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing