Trident 663-00-36GRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327024722), received between Aug 26, 2020 and Aug 26, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

2 other recalls cover devices cleared under the same FDA submission (K033716); they may or may not involve this specific model.

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.

• InjuryAug 26, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  THIS PI IS FOR THE STAGE 1 REVISION SCHEDULED TO TAKE PLACE (B)(6) 2020. AS REPORTED: "PATIENT CAME IN FOR I&I AND [HEAD AND POLY] EXCHANGE. 2 WEEKS LATER PRESENTS TO CLINIC WITH SWELLING AND INCREASED REDNESS. SCHEDULED FOR EXPLANT AND ANTIBIOTIC SPACER ON (B)(6) 2020. COMPLICATING CONDITIONS: JOINT INFECTION."

  Patient problems: Injury; Unspecified Infection

  MAUDE report 10454370 ↗
• InjuryAug 26, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  THIS PI IS FOR THE I&D WITH HEAD AND LINER EXCHANGE ON (B)(6) 2020. AS REPORTED: "PATIENT CAME IN FOR I&I AND [HEAD AND POLY] EXCHANGE. 2 WEEKS LATER PRESENTS TO CLINIC WITH SWELLING AND INCREASED REDNESS. SCHEDULED FOR EXPLANT AND ANTIBIOTIC SPACER ON (B)(6) 2020. COMPLICATING CONDITIONS: JOINT INFECTION."

  Patient problems: Injury; Unspecified Infection

  MAUDE report 10453821 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K033716. One submission often covers many models, so check the product and lot details in each record.

• Z-2810-2015 · Jun 25, 2015 · Terminated
  Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component
• Z-0909-2010 · Feb 17, 2006 · Terminated
  Trident Acetabular Hip System Polyethylene Inserts, Stryker Orthopaedics, multiple sizes, Mahwah, NJ. Intended for use in cementless fixation fro use in total hip arthroplasty to