LCP 241.331Recalls & reported problems
Synthes GmbH · LCP ONE-THIRD TUBULAR PLATE WITH COLLAR 3 HOLES/33MM · Class 2 · Implant
All models of LCP (367)
Data updated Oct 16, 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 10886982166814), received between Oct 24, 2017 and Oct 24, 2017 — classified as 1 injury.
2 other recalls cover devices cleared under the same FDA submission (K011335); 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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Impaired Healing1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 24, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT UNDERWENT REVISION OF A LEFT SIDE ANKLE FUSION ON (B)(6) 2017 DUE TO MALUNION. TWO PLATES AND SIX SCREWS WERE ORIGINALLY IMPLANTED APPROXIMATELY 15 YEARS AGO. THE FUSION HEALED IN MAL-REDUCTION. THE PLATE AND SCREWS WERE REMOVED INTACT, AN OSTEOTOMY PERFORMED, THE DEFORMITY CORRECTED, AND THE ANKLE REFUSED. TWO NEW PLATES AND CORTEX SCREWS WERE IMPLANTED. THE SURGERY WAS SUCCESSFULLY COMPLETED WITH NO DELAY. THE PATIENT OUTCOME WAS REPORTED AS FINE. THIS REPORT IS FOR ONE (1) LCP ONE-THIRD TUBULAR PLATE WITH COLLAR 3 HOLES. THIS IS REPORT 1 OF 8 FOR (B)(4).
Patient problems: Impaired Healing; No Code Available
MAUDE report 6973985 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K011335. One submission often covers many models, so check the product and lot details in each record.
- Z-2816-2020 · Jul 21, 2020 · TerminatedDePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes / 93mm - Product Usage: intended for fixation of fractures, osteotomies and non-unions of clavicle, scapula, ol
- Z-1557-2013 · Feb 22, 2013 · TerminatedSynthes 11-Hole, 1/3 Tubular Plate DCL Plate with Collar, Part Number 241.000.011
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- 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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