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 2828128300 of 29,188 recalls

Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 100/101 Product Usage: The Interface...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...

The Issue: There is a possibility that the screw channel that holds the rod in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Philips Healthcare Inc.

Recalled Item: Philips Essenta DR Recalled by Philips Healthcare Inc. Due to Essenta DR...

The Issue: Essenta DR C-Arm may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...

The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Capintec Inc

Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...

The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...

The Issue: A component within the handle of the Expedium Offset Torque Wrench is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2012· Trek Diagnostic Systems

Recalled Item: VersaTREK Windows Software Recalled by Trek Diagnostic Systems Due to Review...

The Issue: Review of instrument software databases and investigation of two customer...

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

Class III — Low RiskOngoing
Medical DeviceJuly 23, 2012· Cisco Systems Inc

Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...

The Issue: Software anomaly may result in incorrect values and interpretations. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...

The Issue: GE Healthcare become aware of 4 potential issues associated with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· Galil Medical, Inc.

Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...

The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2012· Abbott Point Of Care Inc.

Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...

The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to There is a...

The Issue: There is a potential malfunction in which a miscalculation occurs for images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes Recalled by...

The Issue: Covidien is recalling certain cuffed Shiley tracheostomy tubes due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing