NA 04.112.620Recalls & reported problems
Synthes GmbH · 2.7MM TI VA LCP CLAVICLE PLATE SHAFT/ 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982278944), received between May 24, 2022 and Jan 9, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
- Crack1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 9, 2025Break; Break
THE SURGERY WAS PERFORMED, AND IT WAS REPORTED TODAY THAT ALL FOUR MEDIAL VA 2.7 LOCKING HEAD SCREWS FIXED WITH THE VA CLAVICLE PLATE HAVE BROKEN. REMOVAL OF THE BROKEN SCREWS AND REVISION SURGERY WITH A NEW PLATE IS REQUIRED.
Patient problems: Insufficient Information
MAUDE report 21111979 ↗MalfunctionMay 24, 2022Crack; Crack
ON (B)(6) 2022 DURING AN ORTHOPEDIC PROCEDURE, THE PLATE CRACKED WHILE BEING CONTOURED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A DIFFERENT PLATE, THERE WAS NO SURGICAL DELAY. THIS REPORT IS FOR A 2.7 TI VA LCP CLAV PL SHAFT/ CS1/ LFT. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14492251 ↗
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
Other Plate, fixation, bone devices
- Lapiplasty System 2 SK14Treace Medical Concepts, Inc. · Plate, Fixation, Bone260 reports
- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- 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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