FDA recall Z-2057-2018

Stryker Corporation · Class II · device

Product

3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.

Reason for recall

Inadvertent shipment of expired units.

Distribution

US distribution to Massachusetts only..

Key facts

Status
Completed
Initiation date
2017-12-21
Report date
2018-06-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Jose, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2057-2018