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. 996 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
996 in last 12 months

Showing 34601–34620 of 52,000 recalls

Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Screwdriver Blade Recalled by Synthes (USA) Products LLC Due to DePuy...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #311.039 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Pentax of America Inc

Recalled Item: Ultrasound Video Bronchoscope The EB-1970UK Recalled by Pentax of America...

The Issue: The EB-1970UK Ultrasound Video Bronchoscope shipped between the clearance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Ti Button Plate 7 Holes Recalled by Synthes (USA) Products LLC Due...

The Issue: DePuy Synthes is voluntarily initiating a recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.012 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.211 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.232 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # SD313.011 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part #313.231 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes is...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Synthes (USA) Products LLC

Recalled Item: Part # 313.250 Recalled by Synthes (USA) Products LLC Due to DePuy Synthes...

The Issue: DePuy Synthes is voluntarily initiating this recall due to affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2016· Draeger Medical, Inc.

Recalled Item: Oxylog 3000 Recalled by Draeger Medical, Inc. Due to Isolated episodes of...

The Issue: Isolated episodes of leakage at the check valve were found

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

Class I — Serious Health HazardOngoing
DrugMay 31, 2016· Teva North America

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 30, 2016· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect lot number,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 28, 2016· Par Pharmaceutical

Recalled Item: Pramipexole Dihydrochloride Extended Release Tablets Recalled by Par...

The Issue: Failed Impurities/Degradation Specifications: Par Pharmaceutical is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color D4 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color Impulse brown Recalled by Ivoclar Vivadent, Inc. Due to...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color A3 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color Impulse orange Recalled by Ivoclar Vivadent, Inc. Due to...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color B1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Zenostar MT Color Impulse blue Recalled by Ivoclar Vivadent, Inc. Due to The...

The Issue: The primary packaging of these products may show leaks in individual cases....

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

Class II — Potential Health HazardOngoing