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 18611880 of 29,188 recalls

Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX NEEDLE US Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Connex Vital Signs Monitor (CVSM): Recalled by Baxter Healthcare...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand: Recalled by Baxter...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CP150 Electrocardiograph: Recalled by Baxter Healthcare...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2025· Phasor Health, LLC

Recalled Item: Phasor Drill Recalled by Phasor Health, LLC Due to Drill for use in...

The Issue: Drill for use in neurosurgical procedures may have a reverse battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650C A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 620 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 650 SE Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650 A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650C A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare Carestation 620 SE Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750c A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 650 A1 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing