Acetabular Insert 2099-2258Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327031492), received between Nov 30, 2022 and Nov 30, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryNov 30, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS PI IS FOR REVISION OF THE PATIENT'S LEFT HIP ON (B)(6) 2022. ORIGINALLY REPORTED: "DISLOCATIONS IN A PATIENT AFTER UNDERGOING TOTAL HIP REPLACEMENT SURGERY WITH STRYKER PRODUCTS." RECORDS AND INFORMATION PROVIDED BY LITIGATION COORDINATOR INDICATE THE FOLLOWING PATIENT HISTORY: PRIMARY LEFT HIP IMPLANTATION APPROXIMATELY (B)(6) /2010. REVISION ON (B)(6) 2011 WITH A HEAD AND LINER EXCHANGE. REVISION (B)(6) 2014 DUE TO DISLOCATION, LINER WAS EXCHANGED. REVISION (B)(6) 2022, A CONSTRAINED LINER WAS CEMENTED INTO THE PATIENT. REVISION (B)(6) 2022, ALL STRYKER COMPONENTS REMOVED AND A COMPETITOR HIP WAS IMPLANTED. PER THE LITIGATION COORDINATOR, THE PATIENT IS REFUSING TO PROVIDE ANY ADDITIONAL INFORMATION BEYOND WHAT IS CURRENTLY PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 15885785 ↗
• InjuryNov 30, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THIS PI IS FOR REVISION OF THE PATIENT'S LEFT HIP ON (B)(6) 2014. ORIGINALLY REPORTED: "DISLOCATIONS IN A PATIENT AFTER UNDERGOING TOTAL HIP REPLACEMENT SURGERY WITH STRYKER PRODUCTS." RECORDS AND INFORMATION PROVIDED BY LITIGATION COORDINATOR INDICATE THE FOLLOWING PATIENT HISTORY: PRIMARY LEFT HIP IMPLANTATION APPROXIMATELY ON (B)(6) 2010. REVISION ON (B)(6) 2011 WITH A HEAD AND LINER EXCHANGE. REVISION 11/MAY/2014 DUE TO DISLOCATION, LINER WAS EXCHANGED. REVISION ON (B)(6) 2022, A CONSTRAINED LINER WAS CEMENTED INTO THE PATIENT. REVISION ON (B)(6) 2022, ALL STRYKER COMPONENTS REMOVED AND A COMPETITOR HIP WAS IMPLANTED. PER THE LITIGATION COORDINATOR, THE PATIENT IS REFUSING TO PROVIDE ANY ADDITIONAL INFORMATION BEYOND WHAT IS CURRENTLY PROVIDED.

  Patient problems: Joint Dislocation

  MAUDE report 15885773 ↗