VA-LCP 02.111.720Recalls & reported problems
Synthes GmbH · 2.4MM VA-LCP 2-CLMN VLR DSTL RADIUS PL 7H HD/2H SHAFT/RIGHT · Class 2 · Implant
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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982032256), received between Oct 12, 2020 and Oct 12, 2020 — classified as 1 injury.
2 other recalls cover devices cleared under the same FDA submission (K083694); they may or may not involve this specific model.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Code Available1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 12, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED ON (B)(6) 2020, THE PATIENT UNDERWENT REMOVAL OF HARDWARE DUE TO PAIN. PATIENT WAS ORIGINALLY IMPLANTED WITH ONE (1) VARIABLE LOCKING COMPRESSION PLATE, TWO (2) CORTEX SCREWS, AND FIVE (5) LOCKING SCREWS ON UNKNOWN DATE. THE SURGEON REMOVED THE PLATE AND SCREWS SUCCESSFULLY AND NOTHING WAS BROKEN. THE PATIENT OUTCOME IS UNKNOWN. CONCOMITANT DEVICES REPORTED: 2.4MM VA LOCKING SCREW STARDRIVE 20MM (PART # 02.210.120, LOT # UNKNOWN, QUANTITY 5); 2.7MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 16MM (PART # 202.876; LOT # UNKNOWN, QUANTITY 2). THIS REPORT IS FOR ONE (1) 2.4MM VA-LCP 2-CLMN VLR DSTL RADIUS PL 7H HD/2H SHAFT/RIGHT. THIS IS REPORT 1 OF 8 FOR (B)(4).
Patient problems: No Code Available; Pain
MAUDE report 10667048 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083694. One submission often covers many models, so check the product and lot details in each record.
- Z-2087-2013 · Jul 30, 2013 · TerminatedSynthes 2.4 VA-LCP 2 CLMN VLR DSTL Radius PL 7H HD/3H Shaft/Right Product Usage: Intended for fixation of complex intra-and extra-articular fractures and osteotomies of the dista
- Z-2057-2013 · May 31, 2013 · TerminatedSynthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Torque limiting attachment, 1.2Nm Synthes VA-LCP Distal Radius System is intended for fixation of complex intra- and
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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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