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 2872128740 of 29,188 recalls

Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Optimum Expanse R Grafton is a human bone allograft product Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Gel Multiple Sizes Grafton is a human bone Recalled by Osteotech...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM A-Flex Multiple Sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Optimum Expanse S Multiple sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Crunch Multiple Sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2012· Ge Healthcare It

Recalled Item: The GE Centricity Web Recalled by Ge Healthcare It Due to GE Healthcare has...

The Issue: GE Healthcare has become aware of an issue associated with rejected images...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Bacterin International, Inc.

Recalled Item: Bacterin International Recalled by Bacterin International, Inc. Due to...

The Issue: Expired product was shipped to two customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Standard Administration Kit...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary VSA Stopcock Set Peristaltic...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion Pump Peristaltic Pump System designed for...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Set Peristaltic Pump System...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Administration Kit...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing