FDAFDA · Food and drugs·Recall number Z-2044-2014
Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
Published July 23, 2014 · Recall initiated: May 7, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- MTI Precision Products LLC.
- Distributor
- US Nationwide Distribution in the states of CA, FL, IL, KY, MA, MD NJ, NY, and RI.
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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