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. 2,509 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,509 in last 12 months

Showing 2276122780 of 52,000 recalls

Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.All Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The potential sporadic performance problems may cause scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2019· Zimmer Biomet, Inc.

Recalled Item: Ultra-Drive Irrigation Tubing Assembly Recalled by Zimmer Biomet, Inc. Due...

The Issue: The products do not have sufficient data to support the labeled shelf life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2019· Becton Dickinson & Company

Recalled Item: BD Microtainer Tube w/ BD Microgard Closure Recalled by Becton Dickinson &...

The Issue: The products have been confirmed to have reduced or no additive within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to The...

The Issue: The Vereos PET/CT may have misaligned front and rear covers, which may...

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

Class II — Potential Health HazardOngoing
DrugJune 3, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP 10 mcg Recalled by Glenmark Pharmaceuticals...

The Issue: Defective Delivery System: Estradiol Vaginal Inserts USP plunger is not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium...

The Issue: False elevation of carboxyhemoglobin (COHb) results in blood samples...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Baxter Healthcare Corporation

Recalled Item: REVACLEAR 300 Dialyzer Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Infinium Medical, Inc

Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...

The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing