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. 2,603 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,603 in last 12 months

Showing 1670116720 of 29,188 recalls

Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Tornier, Inc

Recalled Item: AEQUALIS HUMERAL NAIL DRILL BIT Recalled by Tornier, Inc Due to Drill bit...

The Issue: Drill bit tips without new BargerGard tip protector may puncture through...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Navigation, Inc.

Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part...

The Issue: Medtronic has become aware that certain lots of the VCLAS 3MM, 10MM, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...

The Issue: Slot screw had an overall length of 15mm, but per the specification, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 Recalled...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing