NA 02.112.610Recalls & reported problems
Synthes GmbH · 2.7MM VA LCP CLAVICLE PLATE LATERAL/ CS1/ LEFT · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982279347), received between Mar 13, 2023 and Mar 10, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (2 reports).
1 other recall cover devices cleared under the same FDA submission (K201321, K203414); 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 10, 2025Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT ON AN UNKNOWN DATE FOR THE POLYTRAUMA PATIENT, THE CLAVICLE LOCKING PLATE DID NOT LOCK. THE PLATEAU PLATES ON RIGHT SIDE DID NOT LOCK AFTER PUTTING CORTICAL SCREWS IN. THE CORTICAL SCREWS WERE PUT IN FIRST AND THE DRILL GUIDES BENT IN PROCESS OF PUTTING IN THE CANNULATED SCREWS. THERE WAS A SURGICAL DELAY AND AN UNKNOWN ABOUT OF TIME. THERE WAS NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21558865 ↗MalfunctionMar 13, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT ON (B)(6) 2023, THE LOCKING HOLE WAS NOT ENGAGING. THERE WAS NO PATIENT OR PROCEDURE INVOLVEMENT. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE 2.7MM VA LCP CLAVICLE PLATE LATERAL/ CS1/ LEFT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16529703 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K201321, K203414. One submission often covers many models, so check the product and lot details in each record.
- Z-1241-2024 · Jan 24, 2024 · Open, ClassifiedVA-LCP Clavicle Plate 2.7, shaft, CS1, right-Intended for fixation of clavicle bone fragments. Part Number: 02.112.621S
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- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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