RecallRadar

FDA Device recall Z-2044-2014

Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products

On 2014-07-23 the FDA classified a Class II recall of Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products by Mti Precision Products, citing sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2044-2014
ClassificationClass II
Statusterminated
Initiated2012-05-07
Published2014-07-23
Last updated2026-09-13 11:53 UTC
CompanyMti Precision Products
DistributionUS

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.

Identifiers

code_info
P/N Lynx TM20-4H-01: T41202012, T41202013, T41203001, T41203002, T41203003, T41203010, T41204001 to T41204006 P/N…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.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2044-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.