MTI Precision Products LLC.: Medical Device Recall in 2014 - (Recall #: Z-2044-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products

Product Classification:

Class II

Date Initiated: May 7, 2012

Date Posted: July 23, 2014

Recall Number: Z-2044-2014

Event ID: 68570

Reason for Recall:

Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.

Status: Terminated

Product Quantity: 134 devices

Code Information:

P/N Lynx TM20-4H-01: T41202012, T41202013, T41203001, T41203002, T41203003, T41203010, T41204001 to T41204006 P/N Lynx TM20-4H-03 distributed to end user accounts with serial number T41204001 P/N Lynx TM20-2H-03 distributed to Medidenta private labeled as "Meditorque I 20 K" with serial numbers M21203001 to M21203025. P/N Lynx distirbuted to Medidenta private labeled as "Meditorque I 20 K" with serial numbers M21203026 to M21203055. P/N Lynx TM20-4H-01 distributed to Johnson-Promident with serial numbers T41204001-T41204020 P/N Lynx TM20-2H-01 distirbuted to Johnson-Promident with serial numbers T21204001-T21204020.

Distribution Pattern:

US Nationwide Distribution in the states of CA, FL, IL, KY, MA, MD NJ, NY, and RI.

Voluntary or Mandated:

Voluntary: Firm initiated