Recall Z-2044-2014— MTI Precision Products LLC.

Name: FDA recall Z-2044-2014
Creator: U.S. Food and Drug Administration
Published: 2012-05-07

Class II · Terminated

Class II FDA medical device recall by MTI Precision Products LLC., initiated 2012-05-07, terminated 2015-03-12. It names one FDA 510(k) clearance: K940261. Product: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products. Reason: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece..

Recalling firm: MTI Precision Products LLC.
Classification: Class II
Status: Terminated
Initiated: 2012-05-07
Terminated: 2015-03-12
Firm location: Lakewood, NJ, United States

510(k) clearances named in this recall

1 on FDA's record

K940261 — LYNX LOW-SPEED HANDPIECEMti Precision Products·cleared 1994-12-29

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.