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. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2792127940 of 29,188 recalls

Medical DeviceOctober 15, 2012· Toshiba American Medical Systems Inc

Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...

The Issue: It was found that there is a problem with the LCD monitor used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Ossur Americas, Inc.

Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...

The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...

The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· GE Healthcare, LLC

Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Large External Fixation Recalled by Synthes USA HQ, Inc. Due to It...

The Issue: It was discovered internally that there was a discrepancy between the insert...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2012· MOOG Medical Devices Group

Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...

The Issue: The firm is adding an addendum to the operator's manual for Infinity...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...

The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...

The Issue: Firm has received reports from customers that the small pins at the bottom...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Alfa Wassermann, Inc.

Recalled Item: Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann...

The Issue: Inorganic phosphorus assays using System Diluent Lot 155599 may not product...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL...

The Issue: Correlation slope bias and accuracy shift

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

Class III — Low RiskOngoing
Medical DeviceOctober 10, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: There is a risk of lost images during examination.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by...

The Issue: A particular component may not have been fitted during the installation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: PENTRA C200 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA AST CP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: Horiba Medical is recalling the ABX PENTRA AST CP because during the AST...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...

The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2012· Radiometer America Inc

Recalled Item: Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The...

The Issue: RADIOMETER became aware that some membranes may have enzyme residue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method...

The Issue: Siemens Healthcare Diagnostics has confirmed the potential for falsely...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2012· Spacelabs Healthcare, Llc

Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...

The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...

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

Class II — Potential Health HazardOngoing