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Stryker Corporation recalls 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is desi
Recalled June 13, 2018 · FDA recall Z-2057-2018 · Stryker
Hazard
Inadvertent shipment of expired units. · FDA Class II
Units
2 boxes (5 units per box)
Sold at
US distribution to Massachusetts only..
Description
Inadvertent shipment of expired units.
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.
Manufacturer(s)
Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →