FDA Recall
Terminated
Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
Recall: Z-2044-2014
·
Initiated May 7, 2012
Recall
- Recall Number
- Z-2044-2014
- Event Number
- 68570
- Firm
- MTI Precision Products LLC.
- FEI Number
- 2246821
- Product Code
- EFB
- Status
- Terminated
- Root Cause
- Software design (manufacturing process)
- Initiated
- May 7, 2012
- Posted
- July 12, 2014
- Terminated
- March 12, 2015
- Address
- 730 Airport Rd, Suite 1, Lakewood, NJ, 08701-5994
Description
Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
Reason
Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.
Action
MTI notified their customers via e-mail on 5/712 and 5/8/12. MTI sent end-users recall letters on or about 5/9/12.
Distribution
US Nationwide Distribution in the states of CA, FL, IL, KY, MA, MD NJ, NY, and RI.
Quantity
134 devices