Switchcut Reamer 4.5 x 10.0mm w/ Nitinol PassersRecalls & reported problems
T.A.G Medical Products Agricultural Cooperative Association · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10810190013899), received between Oct 22, 2017 and Jan 2, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 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 18, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 2, 2018Break; Break
DURING THE SURGICAL ACT AT THE MOMENT OF MAKING THE BONE TUNNEL WITH THE SWITCH CUT DRILL IT BROKE EVEN BEFORE WE MADE THE TUNNEL
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7156477 ↗MalfunctionOct 22, 2017Break; Break
SWITCH CUT WAS REAMED ON TO GRADE FROM LATERAL CORTEX OF FEMUR IN TO FEMORAL NOTCH. REVERSED REMER TO RETROGRADE REAMER FEMORAL SOCKET AND THE SWITCH CUT BLADE CAUGHT AT THE TOP OF THE NOTCH AND BROKE OFF * 3 TIMES.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6967648 ↗
Other Reamer devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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