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. 2,547 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,547 in last 12 months

Showing 2104121060 of 29,188 recalls

Medical DeviceMarch 2, 2016· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...

The Issue: Radiation emissions which exceeded the limit in the performance standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2016· Alcon Research, Ltd.

Recalled Item: VERION Unit (Vision Planner) Product Usage: The VERION Image Recalled by...

The Issue: Alcon is conducting a voluntary medical device correction of all VERION...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2016· GE Medical Systems, LLC

Recalled Item: SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is Recalled by GE...

The Issue: Ferrous material in the SIGNA Pioneer Table Control Box (TCB) could cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Richard Wolf Medical Instruments Corp.

Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...

The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Karl Storz Endovision, Inc.

Recalled Item: ENDOSCOPE BRUSH- KARL STORZ Flexible Cleaning Brush single-use Recalled by...

The Issue: Endoscope cleaning brush 11276CL may not fit resulting in an inability to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Cardinal Health

Recalled Item: Gomco Style Circumcision Clamp Trays is an instrument used to Recalled by...

The Issue: Two lots of Gomco Style Circumcision Clamp Trays, SSI-0034 and 10-1100...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· Nidek Inc

Recalled Item: RT-5100 (Epic 5100) and RT 3100 : Product Usage: Recalled by Nidek Inc Due...

The Issue: There has been a reoccurrence of an issue on the RT 5100 and RT 3100 of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2016· AMS Diagnostics, LLC

Recalled Item: Medica ISE Module Calibrant A Recalled by AMS Diagnostics, LLC Due to Lot...

The Issue: Lot was not functioning properly and not exhibiting the correct physical...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...

The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...

The Issue: Dialyzer header leak due to possible improper torque

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm has received one report of values for patient height and weight...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· Scottcare Corporation

Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...

The Issue: The firm received a complaint of the battery exploding while recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ab Sciex

Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...

The Issue: Wrong quantitative results may be displayed in a report from the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: syngo X Workplace is a medical workstation for real-time viewing Recalled by...

The Issue: After importing, the segmentation results appear mirrored at the CARTO...

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

Class II — Potential Health HazardOngoing