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. 2,661 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,661 in last 12 months

Showing 1134111360 of 29,188 recalls

Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Talladium Inc

Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...

The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...

The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Hologic, Inc

Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to Tube trays may leak...

The Issue: Tube trays may leak which could invalidate patient results or assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· Integra LifeSciences Corp.

Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...

The Issue: lntegra LifeSciences has identified through a number of complaints that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...

The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...

The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY Recalled by...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System. The EtCO2 module is a capnograph indicated for continuous...

The Issue: Infusion pump component defect may result in interruption of patient monitoring

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Encore Medical, LP

Recalled Item: DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and Recalled by...

The Issue: There is a potential for the retaining pin of the tibial punch handle to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing