VA-LCP 03.115.801Recalls & reported problems
Synthes GmbH · GUIDE BLOCK F/2.4MM VA-LCP VOLAR RIM DSTL RAD PL/7H HD/LT · Class 2
All models of VA-LCP (256)
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 10886982073105), received between Oct 16, 2023 and Oct 16, 2023 — 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. 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
- Material Deformation1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 16, 2023Material Deformation; Material Deformation
DEVICE REPORT FROM JAPAN REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2023, THE PATIENT UNDERWENT AN ORIF SURGERY FOR A DISTAL RADIUS FRACTURE. BEFORE SURGERY, IT WAS FOUND THAT THE GUIDING BLOCK ATTACHMENT SCREW HAD BEEN EXTREMELY BENT. BECAUSE IT WAS SO GREATLY DEFORMED, IT WAS IMPOSSIBLE TO REMOVE THE SCREW AND REPLACE IT WITH A SCREW OF A DIFFERENT SIZE, MAKING IT UNUSABLE. A GUIDING BLOCK WAS BORROWED FROM A NEARBY FACILITY, IT WAS PREPARED IN TIME FOR THE SURGERY. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR A GUIDE BLOCK F/2.4MM VA-LCP VOLAR RIM DSTL RAD PL/7H HD/LT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Insufficient Information
MAUDE report 17944106 ↗
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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 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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