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 2448124500 of 29,188 recalls

Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2014· Nidek Inc

Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...

The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2014· McKesson Technologies, Inc.

Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...

The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...

The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Dental EZ Group Star Dental Division

Recalled Item: Titan T 5K Motor Product Usage: Low-speed motor is used Recalled by Dental...

The Issue: The housing of 5K motor was laser marked incorrectly as a 20K motor. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Biolase Technology Inc

Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...

The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Pentax Medical Company

Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...

The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Heartsine Technologies, Limited

Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...

The Issue: A small number of sealed foil pouches containing the electrodes were found...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: McKesson Medi-Pak Recalled by Medical Action Industries Inc Due to Some of...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Max Barrier Kit Recalled by Medical Action Industries Inc Due to Some of the...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration/Suture Removal Recalled by Medical Action Industries Inc Due to...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration Kit: W/Needles Recalled by Medical Action Industries Inc Due to...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Zimmer Manufacturing B.V.

Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...

The Issue: Two lots of screws were commingled. Screws with etching and machining for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Suture Set Recalled by Medical Action Industries Inc Due to Some of the...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Laceration Trays Recalled by Medical Action Industries Inc Due to Some of...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Medical Action Industries Inc

Recalled Item: Port-A-Cath Tray Recalled by Medical Action Industries Inc Due to Some of...

The Issue: Some of the sterile kits may have incomplete seals which might compromise...

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

Class II — Potential Health HazardOngoing