Dome Hole Plug 2060-0000-1Recalls & reported problems
Howmedica Osteonics Corp. · Acetabular Dome Hole Plug · Class 3 · Implant
Data updated Oct 18, 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 07613327037067), received between Nov 21, 2017 and Nov 21, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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.
Most reported problems
Device problems
- Device Contamination with Chemical or Other Material1
- Material Distortion1
- Packaging Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 21, 2017Device Contamination with Chemical or Other Material; Material Distortion; Packaging Problem; Device Contamination with Chemical or Other Material; Material Distortion; Packaging Problem
IT WAS REPORTED THAT, DURING A THA, WHEN A NURSE OPENED THE PACKAGE, A SURGEON FOUND A THREADLIKE METAL WITH THE PLUG. A SPARE WAS USED INSTEAD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7051262 ↗
Other Prosthesis, hip, semi-constrained (metal cemented acetabular component) devices
- Omnifit 2001-2246Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained (metal cemented acetabular component)1 recall0 reports
- Taperloc Complete Micro Primary Femoral 51-107150Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)41 reports
- Taperloc Complete Micro Primary Femoral 51-107140Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)36 reports
- Dynasty DSBFGD52Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)12 reports
- CONSERVE® 38AM4600Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)8 reports
- CONSERVE® 38AM4804Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)7 reports
- CONSERVE® 38AM4404Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)6 reports
- TRANSCEND® 26000025Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)5 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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