VA-LCPRecalls & reported problems across all models
Synthes GmbH · 256 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
VA-LCP models — page 3
256 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- VA-LCP 02.124.421SScrew, fixation, bone1 report
- VA-LCP 02.127.241Screw, fixation, bone1 report
- VA-LCP 02.127.241SScrew, fixation, bone1 report
- VA-LCP 02.127.251PLATE, FIXATION, BONE1 report
- VA-LCP 02.127.261PLATE, FIXATION, BONE1 report
- VA-LCP 02.127.311PLATE, FIXATION, BONE1 report
- VA-LCP 02.127.340PLATE, FIXATION, BONE1 report
- VA-LCP 02.127.341Screw, fixation, bone1 report
- VA-LCP 02.127.351Screw, fixation, bone1 report
- VA-LCP 02.127.360PLATE, FIXATION, BONE1 report
- VA-LCP 02.211.230Screw, fixation, bone1 report
- VA-LCP 02.211.231Screw, fixation, bone1 report
- VA-LCP 02.211.235PLATE, FIXATION, BONE1 report
- VA-LCP 02.211.244PLATE, FIXATION, BONE1 report
- VA-LCP 02.211.246SScrew, fixation, bone1 report
- VA-LCP 02.211.253Screw, fixation, bone1 report
- VA-LCP 02.211.254SPLATE, FIXATION, BONE1 report
- VA-LCP 03.111.730TEMPLATE1 report
- VA-LCP 03.115.800Screw, fixation, bone1 report
- VA-LCP 03.115.801PLATE, FIXATION, BONE1 report
- VA-LCP 03.118.102PLATE, FIXATION, BONE1 report
- VA-LCP 03.127.008Screw, fixation, bone1 report
- VA-LCP 04.107.202SPLATE, FIXATION, BONE1 report
- VA-LCP 04.107.206Screw, fixation, bone1 report
- VA-LCP 04.110.201PLATE, FIXATION, BONE1 report
- VA-LCP 04.110.204PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.521Screw, fixation, bone1 report
- VA-LCP 04.111.620PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.621PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.640PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.640SPLATE, FIXATION, BONE1 report
- VA-LCP 04.111.641PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.650PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.730PLATE, FIXATION, BONE1 report
- VA-LCP 04.111.731PLATE, FIXATION, BONE1 report
- VA-LCP 04.112.047SPLATE, FIXATION, BONE1 report
- VA-LCP 04.115.751PLATE, FIXATION, BONE1 report
- VA-LCP 04.115.850SScrew, fixation, bone1 report
- VA-LCP 04.117.003SPLATE, FIXATION, BONE1 report
- VA-LCP 04.117.007SPLATE, FIXATION, BONE1 report
- VA-LCP 04.117.204Screw, fixation, bone1 report
- VA-LCP 04.117.303SScrew, fixation, bone1 report
- VA-LCP 04.117.401SPLATE, FIXATION, BONE1 report
- VA-LCP 04.117.502SPLATE, FIXATION, BONE1 report
- VA-LCP 04.117.504SScrew, fixation, bone1 report
- VA-LCP 04.117.704PLATE, FIXATION, BONE1 report
- VA-LCP 04.117.801SScrew, fixation, bone1 report
- VA-LCP 04.117.802SScrew, fixation, bone1 report
- VA-LCP 04.117.901SPLATE, FIXATION, BONE1 report
- VA-LCP 04.211.232SPLATE, FIXATION, BONE1 report
- VA-LCP 04.211.240SScrew, fixation, bone1 report
- VA-LCP 04.211.252Screw, fixation, bone1 report
- VA-LCP 04.211.253PLATE, FIXATION, BONE1 report
- VA-LCP 04.211.254PLATE, FIXATION, BONE1 report
- VA-LCP 04.211.255SScrew, fixation, bone1 report
- VA-LCP 02.111.631KSPlate, fixation, bone1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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