A.L.P.S. mvX™ 770002182Recalls & reported problems
Tyber Medical, LLC · 1.8MM DRILL LONG · Class 1
All models of A.L.P.S. mvX (25)
Data updated Oct 18, 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 00196449012923), received between Oct 11, 2024 and Oct 11, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 11, 2024Fracture; Fracture
FROM COMPLAINANT: FROM STAFF: PATIENT WITH PRIOR ANKLE FRACTURE AND SUBSEQUENT SURGERY TO REMOVE HARDWARE WITH RETAINED BROKEN IMPLANTS LEFT IN PLACE WHO PRESENTED WITH A NEW FRACTURE OF THE SAME ANKLE. DURING SURGERY ( (B)(6) 2024) THE DRILL BIT BROKE AFTER COMING IN CONTACT WITH OTHER HARDWARE. IT WAS BURIED IN THE BONE, AND SURGEON MADE THE DECISION THAT THE RISK OF REMOVING IT OUTWEIGHED THE RISK OF LEAVING IT IN PLACE. RETAINED BROKEN HARDWARE FROM THE PRIOR SURGERIES WAS ALSO LEFT IN PLACE AND THIS HAD BEEN DISCUSSED WITH THE PATIENT BEFORE SURGERY. BOTH THE PATIENT AND HER FAMILY HAVE BEEN NOTIFIED AND AGREE WITH THIS DECISION. FROM OPERATIVE REPORT: OF NOTE THE DURAL-BASED DID BREAK WHILE PLACEMENT OF THE SCREWS DUE TO HARDWARE IN THE DISTAL TIBIA.
Patient problems: Foreign Body In Patient
MAUDE report 20432554 ↗
Other BIT, DRILL devices
- QUICKSET 2274-25-500Depuy Orthopaedics, Inc. · BIT, DRILL1,985 reports
- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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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