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. 2,083 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,083 in last 12 months

Showing 50815100 of 52,000 recalls

FoodJuly 17, 2024· Kenny's Farmhouse Cheese

Recalled Item: Kenny's Farmhouse Cheese - St. Jerome packaged in plastic vacuum 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
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Boston Scientific Neuromodulation Corporation

Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...

The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...

The Issue: The Spectrum WBM may fail to auto-document infusion status information back...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Mazor Robotics Ltd

Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...

The Issue: Software anomalies which can result in two separate issues: A lagging screen...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2024· Beckman Coulter Biomedical GmbH

Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...

The Issue: The adhesive joint between the plastic socket and metal component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 16, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE3.0MM ANG DUAL Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK SATINSLIT FULL HANDLE2.75MM ANG SG Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25GA VALVED ENTRY SYSTEM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: ClearCut Sideport Knife Dual Bevel 1.2mm...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.75MM ANG DUA Recalled...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: Alcon Custom Pak Model/Catalog Number: Many Software Version:...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing