DHS 281.031SRecalls & reported problems
Synthes GmbH · 130 DEG DHS PLATE-STD BARREL 3 HOLES/62MM-STERILE · Class 2 · Implant
Data updated Oct 13, 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 10886982176493), received between Oct 10, 2018 and Oct 10, 2018 — 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- 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 10, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE DHS PLATE, LAG SCREW AND CANNULATED SCREW WERE INTACT, THE TWO (2) CORTEX SCREWS WERE BROKEN AT THE HEAD.
Patient problems: No Code Available
MAUDE report 7953996 ↗
Other DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT devices
- 13 X 90mm LAG FASTENER 324-13090Osteocentric Technologies, Inc. · Device, Fixation, Proximal Femoral, Implant1 report
- CONQUEST FN 71179203Smith & Nephew, Inc. · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 280.295Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- CONQUEST FN 75808095Smith & Nephew, Inc. · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- CONQUEST FN 71179213Smith & Nephew, Inc. · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 280.305Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 280.285SSynthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
- DHS 281.504Synthes GmbH · DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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