FDA Device recall Z-2044-2014
Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
- FDA Device
- Class II
- terminated
- Published 2014-07-23
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
| Agency | FDA Device |
|---|---|
| Recall number | Z-2044-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-05-07 |
| Published | 2014-07-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Mti Precision Products |
| Distribution | US |
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
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