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Dri-Lok

STRYKER CORPORATION · Model 3910090006 · UDI-DI 07613327061109

NBH Prescription
2
510(k) clearances
5,221
Adverse events
55
Recalls
297
Facilities

Description

Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator

Recalls

DateFirmReason
2020-09-21Smith & Nephew, Inc.The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system
2019-06-25BioPro, Inc.Manufacturing flaw in the sterile barrier system

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.