NA 04.112.821SRecalls & reported problems
Synthes GmbH · 2.7MM TI VA LCP HOOK PLATE SHORT/ 9MM/ RIGHT/ STERILE · 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 10886982279743), received between Sep 13, 2024 and Sep 13, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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
- Break1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 13, 2024Break; Break
IT WAS REPORTED THAT ON (B)(6) 2024, THE PATIENT UNDERWENT AN ORIF WITH THE CLAVICLE HOOK PLATE FOR THE DISTAL CLAVICLE FRACTURE. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. ONE WEEK AFTER THE SURGERY, THE ACROMION WAS TORN. THE HOOK PART DISLOCATED, AND THE SCREW WAS BROKEN OFF. ON (B)(6) 2024, A REVISION SURGERY WILL BE PERFORMED WITH OTHER COMPANY¿S PLATE. THE EVENT IS LIKELY TO BE PATIENT-INDUCED. ALTHOUGH THE PATIENT SAID THAT THEY DID NOT FALL OR RAISE ARM, THERE IS SUSPICION. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR ONE (1) 2.7MM TI VA LCP HOOK PLATE SHORT/ 9MM/ RIGHT/ STERILE. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4).
Patient problems: Unspecified Tissue Injury
MAUDE report 20218367 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive 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-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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