TRUMATCH 42-0906Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295384816), received between Jul 17, 2020 and Apr 17, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Incorrect Measurement” (3 reports).

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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 17, 2026Device-Device Incompatibility; No Apparent Adverse Event

  IT WAS REPORTED THAT THE SCRUB TECHS WERE HAVING ISSUES ATTACHING THE 2-PRONGED ATTACHMENT PIECE TO THE TIBIAL PIN BLOCKS BECAUSE THE HOLES SEEM TO BE MANUFACTURED SMALLER THAN PREVIOUSLY. IT HAS ALSO CREATED ISSUES FOR THE SURGEONS NOT BEING ABLE TO VISUALIZE THEIR ALIGNMENT AND SLOPE BECAUSE THE METAL PIECE WON¿T SIT FLUSH. A COUPLE OF BLOCKS HAVE BROKEN AT THAT JUNCTURE, AS THE SCRUB TECHS USE METAL INSTRUMENTS ATTEMPTING TO TAP IT IN FLUSH.

  Patient problems: Insufficient Information

  MAUDE report 24916573 ↗
• MalfunctionApr 10, 2026Nonstandard Device; Device-Device Incompatibility

  IT WAS REPORTED THAT THE SCRUB TECHS WERE HAVING ISSUES ATTACHING THE 2-PRONGED ATTACHMENT PIECE TO THE TIBIAL PIN BLOCKS BECAUSE THE HOLES SEEM TO BE MANUFACTURED SMALLER THAN PREVIOUSLY. IT HAS ALSO CREATED ISSUES FOR THE SURGEONS NOT BEING ABLE TO VISUALIZE THEIR ALIGNMENT AND SLOPE BECAUSE THE METAL PIECE WON¿T SIT FLUSH. A COUPLE OF BLOCKS HAVE BROKEN AT THAT JUNCTURE, AS THE SCRUB TECHS USE METAL INSTRUMENTS ATTEMPTING TO TAP IT IN FLUSH.

  Patient problems: Insufficient Information

  MAUDE report 24840930 ↗
• MalfunctionFeb 2, 2021Incorrect Measurement; Incorrect Measurement

  DURING BILATERAL TKA, THERE WAS A MAJOR ISSUE WITH THE EXTERNAL ROTATION ON BOTH FEMORAL BLOCKS. THE BLOCKS WERE EXTERNALLY ROTATED. AFTER NOTICING THERE WAS TOO MUCH EXTERNAL ROTATION, SURGEON HAD TO USE THE REGULAR SIZING DEVICE TO DIAL IT BACK DOWN TO NORMAL, DELAYING EACH KNEE BY ABOUT 10 MINUTES."

  Patient problems: Insufficient Information

  MAUDE report 11265643 ↗
• MalfunctionJul 17, 2020Incorrect Measurement; Incorrect Measurement

  IT WAS REPORTED AS " EVENT DESCRIPTIONS: TMK23137, KK, NOT ENOUGH EXTERNAL ROTATION IN SURGERY TMK23228, MT, TOO MUCH EXTERNAL ROTATION IN SURGERY TMK23258, JG, LEFT KNEE, FOLLOWING UP ON ROTATION ISSUE."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10290243 ↗
• MalfunctionJul 17, 2020Incorrect Measurement; Incorrect Measurement

  IT WAS REPORTED AS " EVENT DESCRIPTIONS: TMK23137, KK, NOT ENOUGH EXTERNAL ROTATION IN SURGERY. TMK23228, MT, TOO MUCH EXTERNAL ROTATION IN SURGERY. TMK23258, JG, LEFT KNEE, FOLLOWING UP ON ROTATION ISSUE."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10290230 ↗