TRANSCEND® 26000025Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI M684260000251), received between Jul 3, 2019 and Jun 21, 2024 — classified as 5 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryJun 21, 2024Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT WAS REVISED DUE TO ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS. SRNJR NUMBER: (B)(4) SIDE: L GENDER: F NON MPO DEVICES: 99961735 ZMR CONE A BODY PROXIMAL STEM LENGTH 80MM 40X35MM NECK AND 99821713 TAPER STEM 17MM X 135MM (ZIMMER BIOMET)

  Patient problems: Metal Related Pathology

  MAUDE report 19586738 ↗
• InjuryDec 29, 2021Naturally Worn; Noise, Audible; Naturally Worn; Noise, Audible

  ALLEGEDLY, ON (B)(6) ON 2021, PATIENT PRESENTED TO (B)(6) WITH COMPLAINTS OF RIGHT HIP PAIN, WEAKNESS, AND SQUEAKING. AN X-RAY REVEALED MARKED SUPERIOR MIGRATION OF THE FEMORAL HEAD IN THE ACETABULUM, SOME CONTACT BETWEEN THE BALL AND THE TITANIUM SHELL, CUP QUITE VERTICAL AND SUSPECTED LOOSENING, THE CUP MIGRATED MORE VERTICAL WITH RISK OF THE FEMORAL HEAD ESCAPING, AND WITH PROBABLE METAL-ON-METAL IN THE REVISION SURGERY PERFORMED ON PATIENT ON (B)(6) ON 2021, HIS OPERATING SURGEON FOUND FAILURE OF THE RIGHT TOTAL HIP PROTHESIS WITH WEAR OF THE LINER, DISSOCIATION AND METALLOSIS FROM METAL-ON-METAL CONTACT WITH THE FEMORAL HEAD AND ACETABULAR COMPONENT WITH ABDUCTOR NECROSIS. IN THE REVISION SURGERY, THE WRIGHT MEDICAL DYNASTY SHELL, LINER, GLADIATOR STEM, AND FEMORAL HEAD, WERE EACH REMOVED AND REPLACED WITH DEVICES NOT MANUFACTURED BY WRIGHT MEDICAL.

  Patient problems: Metal Related Pathology; Pain

  MAUDE report 13114326 ↗
• InjuryAug 30, 2021Material Disintegration; Malposition of Device; Material Disintegration; Malposition of Device

  ALLEGEDLY, THE PATIENT WAS REVISED DUE TO LINER WEAR, DISASSOCIATION AND METALLOSIS FROM METAL ON METAL CONTACT WITH THE FEMORAL HEAD AND ACETABULAR COMPONENT. (RIGHT HIP).

  Patient problems: Insufficient Information

  MAUDE report 12388315 ↗
• InjurySep 20, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  ALLEGEDLY, PATIENT PRESENTED WITH PAIN. REMOVAL OF DYNASTY CUP FOR LOOSENING. NO ACUTE INJURY OF PATIENT. MPO IMPLANTS WERE REMOVED AND REPLACED WITH ANOTHER SUPPLIERS IMPLANTS.

  Patient problems: Pain

  MAUDE report 9100718 ↗
• InjuryJul 3, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

  ALLEGEDLY, PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2016. THE SURGEON FOUND A DISSOCIATION AFTER SURGERY AND MENTIONED EXCESSIVE STRESS, MAY HAVE OCCURRED DURING AGRICULTURAL WORK. THE SURGEON PERFORMED REVISION SURGERY ON (B)(6) 2019. WE WILL NOT RETURN AT THIS TIME.

  Patient problems: No Information

  MAUDE report 8758336 ↗