FDA Device recall Z-2057-2018
3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box
- FDA Device
- Class II
- completed
- Published 2018-06-13
On 2018-06-13 the FDA classified a Class II recall of 3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box by Stryker, citing inadvertent shipment of expired units.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2057-2018 |
| Classification | Class II |
| Status | completed |
| Initiated | 2017-12-21 |
| Published | 2018-06-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker |
| Distribution | MA |
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.
Identifiers
| upc | 07613327055795 |
|---|---|
| code_info | Lot No. 14239AG2, UPC 07613327055795. The expiration date marked on the box is August 2018, but it should be August 2016. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2057-2018%22
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