Tools - Screws XTNDRGUIDERecalls & reported problems
Trimed, INC. · Peg Guide Extender · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188112850), received between Mar 20, 2018 and Mar 20, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Integrity Problem1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2018Material Integrity Problem; Material Integrity Problem
ON (B)(6) 2018, TRIMED WAS NOTIFIED OF A PEG EXTENDER THAT WAS FOUND TO HAVE STARTED TO RUST. THE REP REPORTED THAT THIS FEEDBACK WAS NOT ASSOCIATED WITH A CLINICAL EVENT, AND THERE WAS NO PATIENT INVOLVEMENT. THIS IS THE SEVENTH COMPLAINT OF THIS KIND FOR THIS PART.
Patient problems: No Patient Involvement
MAUDE report 7355989 ↗
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- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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