Alpine Hip System 700-0014Recalls & reported problems
Ortho Development Corporation · STD Size 14 Stem Press-Fit · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00822409000067), received between Feb 20, 2018 and May 5, 2023 — classified as 1 injury, 1 malfunction.
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 Problem2
Patient problems
- Arthralgia1
- No Code Available1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DURING TOTAL HIP ARTHROPLASTY, A BONE FRACTURE WAS OBSERVED AT THE TRANSVERSE CONDYLE THAT WAS REINFORCED WITH CEMENT AND TWO SCREWS.
Patient problems: Arthralgia
MAUDE report 16880322 ↗MalfunctionFeb 20, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A PATIENT UNDERWENT CEMENTLESS BIPOLAR SURGERY ON (B)(6) 2016. THE SURGEON NOTED SUBSIDENCE IN A POST-OP VISIT AND DECIDED TO CONTINUE TO MONITOR. ON (B)(6) 2017, THE PATIENT WAS REVISED WITH A BIPOLAR STEM FROM A DIFFERENT MANUFACTURER. THE SURGEON SUSPECTED THE SUBSIDENCE WAS CAUSED BY SELECTING A STEM SIZE THAT WAS TOO SMALL.
Patient problems: No Code Available
MAUDE report 7283660 ↗
Other Prosthesis, hip, hemi-, femoral, metal devices
- UHR UH1-48-28Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal2 recalls3 reports
- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3115United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- STAGEONE 431207Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3111United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- ACTIS 101011050Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal73 reports
- UHR UH1-46-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
- UHR UH1-45-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.