FDA recall Z-0284-2018

Zimmer Dental Inc · Class II · device

Product

Tapered Screw-Vent MTX Model TSVTB11

Reason for recall

Some implant vial caps in the recalled implant lot may inadvertently crack as the result of a manufacturing assembly condition.

Distribution

US, Canada, France, Italy, Spain, Germany

Key facts

Status
Terminated
Initiation date
2017-11-20
Report date
2017-12-27
Termination date
2024-02-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Carlsbad, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0284-2018