Tools - UOS UOSG-A-2Recalls & reported problems
Trimed, INC. · Saw Guide A, 2mm · 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 00842188112256), received between Oct 22, 2025 and Oct 22, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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.
Reports received per month
Most reported problems
Device problems
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 22, 2025Material Deformation; Material Deformation
SALES REP REPORTED ON 23SEP2025 THAT WHILE COVERING A (B)(6) CASE WITH A SURGEON AND A (B)(6) RESIDENT (LEADING), THEY ENCOUNTERED AN ISSUE WITH THE 2MM A CUT GUIDE. IT WAS STATED THAT FOLLOWING SOME DIFFICULTY MAKING THE INITIAL CUT, THE SURGEON NOTICED THAT THE A CUT GUIDE WAS SLIGHTLY BENT. IT WAS UNCLEAR IF IT MIGHT HAVE BEEN SLIGHTLY BENT INITIALLY OR IF SOMETHING DURING THE CASE CAUSED THE GUIDE TO BEND. REGARDLESS, THEY DECIDED TO REVISE AFTER MAKING THE B CUT RESULTING IN A LARGER WEDGE THAN PLANNED. IT WAS STATED THAT THE DEVICE CAME IN CONTACT WITH THE PATIENT PER PLANNED PROCEDURE HOWEVER THIS CAUSED OVER A 20-MINUTE DELAY IN SURGERY DUE TO THE REPEATED CUT REVISION. THE REP PROVIDED ADDITIONAL INFORMATION ON (B)(6) 2025 THAT PERMANENT DAMAGE/IMPAIRMENT IS UNCLEAR DUE TO POSSIBLE NEGATIVE ULNAR VARIANCE SEQUELAE. HE STATED THAT HE ASSUMES THE OSTEOTOMY WILL HEAL DUE TO ADEQUATE COMPRESSION (UNCLEAR IF THERE MAY BE SUBSEQUENT SYMPTOMS/IATROGENIC RADIOCARPAL OVERLOAD), HOWEVER THERE WAS NO MENTION OF POSSIBLE FURTHER INTERVENTION. THE SURGEON DID NOT MENTION ANY SUSPECTED NEED FOR FURTHER INTERVENTION FOLLOWING THE CASE AND HE DID NOT APPEAR PARTICULARLY PLEASED WITH THE E
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23362511 ↗
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- DJO SURGICAL 342-10-705Encore Medical, L.P. · Guide, Surgical, Instrument1 recall51 reports
- DJO SURGICAL 341-10-707Encore Medical, L.P. · Guide, Surgical, Instrument81 reports
- NA 03.010.404Synthes GmbH · Guide, surgical, instrument73 reports
- DJO SURGICAL 341-14-708Encore Medical, L.P. · Guide, Surgical, Instrument1 recall22 reports
- DJO SURGICAL 341-10-711Encore Medical, L.P. · Guide, Surgical, Instrument1 recall16 reports
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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