Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products — Class II medical device recall Z-2044-2014
Terminated recall by MTI Precision Products LLC., reported 2014-07-23, distributed nationwide. Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.
| Recall number | Z-2044-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MTI Precision Products LLC., Lakewood, NJ, United States |
| Recall initiated | 2012-05-07 |
| Classified | 2014-07-12 |
| Reported by FDA | 2014-07-23 |
| Terminated | 2015-03-12 |
| Distributed | Nationwide (US) |
| Quantity | 134 devices |
| Serial numbers | M21203001, M21203025, M21203026, M21203055, T21204001-T21204020, T41204001, T41204001-T41204020 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2044-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.