DCP 243.57Recalls & reported problems
Synthes (U.S.A.) LP · 2.0MM DCP® PLATE 7 HOLES/37MM · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982169143), received between Feb 5, 2018 and Feb 5, 2018 — classified as 1 malfunction.
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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2018Break; Break
IT WAS REPORTED THAT THE PATIENT, A FIVE (5) KILOGRAM (B)(6) DOG, HAD A REVISION PROCEDURE ON (B)(6) 2018 DUE TO A BROKEN TIBIAL PLATE. THE PATIENT WAS IMPLANTED WITH THE PLATE FOR A FRACTURE TIBIAL REPAIR ON (B)(6) 2017 WHEN THE OWNER REALIZED THE DOG COULD NOT STAND/BEAR ITS WEIGHT. THE DOG WAS EXAMINED AND X-RAYS REVEALED FRACTURE OF THE PLATE. THERE WERE NO SIGNS OF IMPACT, CONTUSION OR TRAUMA TO DOG. THE PLATE WAS REMOVED AND REPLACED. SURGICAL DELAY AND PATIENT OUTCOME IS UNKNOWN. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR ONE (1) PLATE. (B)(4).
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7242738 ↗
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- 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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