VA-LCP 02.124.411SRecalls & reported problems
Synthes GmbH · 4.5MM VA-LCP CURVED CONDYLAR PLATE/10HOLE/230MM/LT-STER · 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 10886982042842), received between Aug 27, 2018 and Aug 27, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K083025, K110354); 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
- Break1
Patient problems
- Failure of Implant1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 27, 2018Break; Break
IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY ON (B)(6) 2018, DUE TO A BROKEN VARIABLE ANGLE (VA) - LOCKING COMPRESSION PLATE (LCP) CURVED CONDYLAR PLATE. THE PATIENT WAS EXPERIENCING PAIN. ON AN UNKNOWN DATE, AN X-RAY WAS TAKEN AND REVEALED A BROKEN PLATE. TEN (10) UNKNOWN SCREWS WERE ALSO REMOVED FULLY INTACT. ORIGINAL IMPLANT DATE WAS (B)(6) 2018. THE PATIENT WAS REVISED TO STRYKER DEVICES. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO ADDITIONAL MEDICAL INTERVENTION WAS NECESSARY. THE PATIENT WAS STABLE FOLLOWING SURGERY. CONCOMITANT DEVICES REPORTED: UNKNOWN SCREWS (PART NUMBER: UNKNOWN, LOT NUMBER: UNKNOWN, QUANTITY: 10). THIS REPORT IS FOR ONE (1) 4.5MM VA-LCP CURVED CONDYLAR PLATE/10HOLE/230MM/LT-STER. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: Failure of Implant; Pain
MAUDE report 7820415 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083025, K110354. One submission often covers many models, so check the product and lot details in each record.
- Z-1125-2014 · Feb 5, 2014 · TerminatedSynthes 5.0mm Variable Locking Screw This device is part of the Variable Angle Locking Compression Plate family and this technology included variable angle Combi holes in the plat
- Z-0401-2014 · May 29, 2013 · TerminatedSynthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER Synthes 4.5MM TI VA-LCP CRVD Condylar Plate/6H/159MM/RT-STER is used for buttressing multi fragmentary diatal femur fra
Other condylar plate fixation Implant devices
- VA-LCP 03.231.007Synthes GmbH · condylar plate fixation Implant56 reports
- VA-LCP 03.231.005Synthes GmbH · condylar plate fixation Implant37 reports
- VA-LCP 02.124.416Synthes GmbH · condylar plate fixation Implant24 reports
- VA-LCP 02.124.413Synthes GmbH · condylar plate fixation Implant14 reports
- VA-LCP 02.124.408Synthes GmbH · condylar plate fixation Implant12 reports
- NA 02.231.675Synthes GmbH · condylar plate fixation Implant11 reports
- NA 02.231.260Synthes GmbH · condylar plate fixation Implant10 reports
- NA 02.231.275Synthes GmbH · condylar plate fixation Implant10 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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