Recall Z-2057-2018— Stryker Corporation
Class II · Completed
Class II FDA medical device recall by Stryker Corporation, initiated 2017-12-21. FDA's recall record names no specific 510(k) clearance for this event. 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: Inadvertent shipment of expired units..
- Recalling firm
- Stryker Corporation
- Classification
- Class II
- Status
- Completed
- Initiated
- 2017-12-21
- Firm location
- San Jose, CA, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.