Reported Jul 23, 2014 · Terminated

Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products

MTI Precision Products LLC.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MTI Precision Products LLC. · 730 Airport Rd Suite 1 · Lakewood, NJ · 08701-5994

Is this the product you have?

  • Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
Lot codes and dates

6 of 6 products

Products covered by this recall
#Product as published
1P/N Lynx TM20-4H-01: T41202012, T41202013, T41203001, T41203002, T41203003, T41203010, T41204001 to T41204006
2P/N Lynx TM20-4H-03 distributed to end user accounts with serial number T41204001
3P/N Lynx TM20-2H-03 distributed to Medidenta private labeled as "Meditorque I 20 K" with serial numbers M21203001 to M21203025.
4P/N Lynx distirbuted to Medidenta private labeled as "Meditorque I 20 K" with serial numbers M21203026 to M21203055.
5P/N Lynx TM20-4H-01 distributed to Johnson-Promident with serial numbers T41204001-T41204020
6P/N Lynx TM20-2H-01 distirbuted to Johnson-Promident with serial numbers T21204001-T21204020.
Amount recalled
134 devices

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 12, 2015 · Data as of Sep 19, 5:24 PM UTC

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