Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental recall
Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
Why was Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental recalled?
Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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.
- Product
- Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products
- Recalling firm
- MTI Precision Products LLC.
- Quantity
- 134 devices
- Distribution
- US Nationwide Distribution in the states of CA, FL, IL, KY, MA, MD NJ, NY, and RI.
- Recall date
- July 23, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)