Secur-Fit J6052-0830Recalls & reported problems
Howmedica Osteonics Corp. · Cementless Hip Stem · Class 2 · Implant
All models of Secur-Fit (45)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327101768), received between Sep 24, 2019 and Sep 1, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Degraded” (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
- Degraded1
- Fracture1
- Insufficient Device Problem Information1
- Loss of Osseointegration1
- Osseointegration Problem1
Patient problems
- Injury2
- Inadequate Osseointegration1
- Inflammation1
- Reaction1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 1, 2020Degraded; Insufficient Device Problem Information; Degraded; Insufficient Device Problem Information
THERE WERE SOME AREAS WHERE THE TISSUE WAS DISCOLORED BLACK DURING THE REMOVAL OPERATION, AND THERE WERE FINDINGS LIKE ARMD. CHECK TO SEE IF THERE WAS ANY IMPINGEMENT ON THE SHELL AND STEM NECK, AND IF THERE ARE ANY SCRATCHES ON THE STEM NECK. NO VISIBLE DAMAGE TO THE STEM NECK WAS FOUND DURING SURGERY. UPDATE: "LOOSENING, SUSPECTED INFECTION. INTRAOPERATIVE EXAMINATION SHOWED NO INFECTION."
Patient problems: Inflammation; Injury; Reaction
MAUDE report 10480221 ↗InjurySep 24, 2019Fracture; Loss of Osseointegration; Osseointegration Problem; Fracture; Loss of Osseointegration; Osseointegration Problem
ON (B)(6) 2009: RESURFACING HEAD (181142/MMT) AND METAL ON METAL CUP 48MM CUP FOR 42MM HEAD (172485/ MMT) WAS IMPLANTED. ON (B)(6) 2010: THE FEMORAL NECK FRACTURE WAS OCCURRED AND THA WAS DONE WITH SSF STEM AND MODULAR HEAD V40 TAPER 42MM -4MM NECK LENGTH (179-242/MMT). ON (B)(6) 2019: REVISION SURGERY OF ALL DEVICES WERE DONE BECAUSE THE LOOSENING AND ARMD WAS OCCURRED.
Patient problems: Inadequate Osseointegration; Injury
MAUDE report 9109430 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, uncemented devices
- LFIT 6260-9-136Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented166 reports
- Trident 623-00-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented112 reports
- Accolade 6021-0435Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented88 reports
- EXETER 0580-1-044Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented1 recall22 reports
- Endo-Model SL Knee Prosthesis System 16-2840/02WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall17 reports
- Endo-Model SL Knee Prosthesis System 16-2840/05WALDEMAR LINK GmbH & Co. KG · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented1 recall12 reports
- Trident 623-10-36EHowmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented57 reports
- LFIT 6260-9-336Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, uncemented56 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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