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Acetabular Insert 2099-2252Recalls & reported problems

Howmedica Osteonics Corp. · Acetabular Insert · Class 2 · Implant

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327031447), received between Apr 11, 2019 and Apr 11, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

  1. Jul 30, 2026Open, Classified

    Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

    Z-3201-2026 · Root cause: Process change control · FDA record ↗

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • Injury1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 11, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated

    BHA WAS DONE WITH NON STRYKER STEM AND BIPOLAR CUP ABOUT 8 YEARS AGO. THE HEAD AND CUP WAS DISLOCATED AND REVISON SURGERY WAS DONE WITH CONSTRAINED LINER AT (B)(6) 2019. STEM AND HEAD WAS NOT CHANGED. AT (B)(6) 2019, IT WAS DISLOCATED AND STEM WAS REMOVED. THE PATIENT HAD PARALYSIS AND BEDRIDDEN. THE REVISION SURGERY WAS NOT PLANED AT THIS TIME.

    Patient problems: Injury

    MAUDE report 8505919 ↗

Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.