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.
Reported: June 13, 2018 Initiated: December 21, 2017 #Z-2057-2018
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.
Details
- Recalling Firm
- Stryker Corporation
- Units Affected
- 2 boxes (5 units per box)
- Distribution
- US distribution to Massachusetts only..
- Location
- San Jose, CA
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Stryker Corporation. Units affected: 2 boxes (5 units per box).
Why was this product recalled? ▼
Inadvertent shipment of expired units.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 13, 2018. Severity: Moderate. Recall number: Z-2057-2018.
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