FDA Device Intelligence
HomeSmith & Nephew, Inc. › TWINFIX

TWINFIX

Smith & Nephew, Inc. · Model 7209115 · UDI-DI 03596010448491

NBH Prescription
2
510(k) clearances
5,126
Adverse events
55
Recalls
296
Facilities

Description

TWINFIX 6 INCH DRILL GUIDE - 6 INCH X 5 MM SPIKE TIP FOR 5.0 MM TITANIUM ANCHOR

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

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.