NA 02.130.150Recalls & reported problems
Synthes GmbH · 1.3MM LOCKING STRAIGHT PLATE 6 HOLES · Class 2 · Implant
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 10886982044389), received between Apr 11, 2024 and Apr 11, 2024 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Joint Contracture1
- Loss of Range of Motion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
POST MARKET STUDY REPORTED: IN COLLABORATION WITH DEPUY SYNTHES, DR. , TOGETHER WITH (B)(6) CLINIC FOUNDATION (B)(6) DATABASE DESIGNERS, PROGRAM MANAGERS, RESEARCH ASSISTANTS, AND BIOSTATISTICIANS, HAS DEVELOPED A REPORT THAT SUMMARIZES SAFETY AND EFFECTIVENESS DATA ON (B)(4) PATIENTS WHO UNDERWENT HAND SURGERY AT CCF BETWEEN 2008 AND 2023 UTILIZING DEPUY SYNTHES (DPS) HAND PLATES. IMPLANTS INVOLVED WERE LCP COMPACT HAND PLATES OR VA LOCKING HAND SYSTEM. 3 PATIENTS WERE NOTED TO HAVE MORE THAN ONE PLATE IMPLANTED. DPS SCREWS WERE INVOLVED. PATIENT #6 20-YEAR-OLD FEMALE WAS IMPLANTED WITH A LOCKING HAND PLATES, STRAIGHT (02.130.150) WITH 6 SCREWS. POST OP COMPLICATION WAS REPORTED FOR PERSISTENT LIMITED ROM DUE TO POST-ORIF CONTRACTURE. TREATMENT: LEFT SMALL FINGER MCP CAPSULAR RELEASE; 1. OPEN EXTENSOR TENOLYSIS LEFT SMALL FINGER. 2. OPEN METACARPOPHALANGEAL JOINT CAPSULAR RELEASE, LEFT SMALL FINGER. THIS REPORT IS FOR ONE 1.3MM LOCKING STRAIGHT PLATE 6 HOLES FOR (B)(4).
Patient problems: Joint Contracture; Loss of Range of Motion
MAUDE report 19088927 ↗
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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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