DHS 281.440Recalls & reported problems
Synthes GmbH · 150 DEG DHS® PLATE-STANDARD BARREL 4 HOLES/78MM · Class 2 · Implant
All models of DHS (57)
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 10886982177360), received between Apr 21, 2020 and Apr 21, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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
- Material Deformation1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 21, 2020Material Deformation; Material Deformation
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED DURING INSPECTION OF TWO (2) DYNAMIC HIP SCREW (DHS) LOANER IMPLANT SETS TO THE HOSPITAL, THE PROCESSING DEPARTMENT NOTICED THERE IS DAMAGE ON ONE FLAT SIDE OF EACH DHS BARREL PLATE. AFTER TWO (2) ADDITIONAL WASHES/STERILIZATION, THE DAMAGE WAS STILL THERE. UPON CLOSER INSPECTION, IT LOOKS LIKE THEY HAVE BEEN SCRATCHED OR ETCHED. NO PATIENT INVOLVEMENT. THIS IS REPORT 1 OF 1 FOR (B)(4). THIS COMPLAINT IS LINKED TO (B)(4).
Patient problems: No Patient Involvement
MAUDE report 9980902 ↗
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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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