Trilogy® 6200-50-22Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024118065), received between Jul 6, 2022 and Dec 18, 2023 — classified as 3 injuries.

The most frequently reported specific device problem is “Material Erosion” (1 report).

16 other recalls cover devices cleared under the same FDA submission (K934765); 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryDec 18, 2023Material Erosion; Material Erosion

  UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE AS THERE WAS NO ALLEGATION AGAINST THE DEVICE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

  Patient problems: Metal Related Pathology; Pain

  MAUDE report 18345756 ↗
• InjuryOct 31, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT REPORTED LEFT HIP ATROPHY, TENDERNESS, PAIN AND CREPITUS WITH ROM APPROXIMATELY 2 YEARS POST TOTAL HIP ARTHROPLASTY. THE PATIENT RECEIVED AN INJECTION FOR THE PAIN AND BURSITIS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Muscle/Tendon Damage; Pain

  MAUDE report 15699147 ↗
• InjuryJul 6, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN IN THE UPPER SIDE OF THE HIP AND ALLEGED SENSATION OF THE TENDON MOVING WITHIN THE JOINT APPROXIMATELY 11 YEARS POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pain

  MAUDE report 14939009 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K934765. One submission often covers many models, so check the product and lot details in each record.

• Z-1684-2016 · May 4, 2016 · Terminated
  Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone screw 6.5x15 selftap 00625006515 Bone screw 6.5x20 selftap 0062500
• Z-1145-2016 · Jan 11, 2016 · Terminated
  Product 47 consists of all product under product code: LPH and same usage: Item no: 611004022 MODULAR CUP 10 DEGREE LIN 611004428 MODULAR CUP 10 DEGREE LIN 611004628 MODULAR CUP
• Z-1161-2016 · Jan 11, 2016 · Terminated
  Product 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM O 620004220 TRILOGY ACET SHELL 42MM O 620004420 TRILOGY ACET
• Z-1115-2016 · Jan 11, 2016 · Terminated
  Product 17 consists of all product under product code: LPH and same usage: Item no: 625004515 BONE SCREW 4.5X15 SELF-TA 625004520 BONE SCREW 4.5X20 SELF-TA 625004525 BONE SCREW
• Z-1123-2016 · Jan 11, 2016 · Terminated
  Product 25 consists of all product under product code: LPH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON 234703206 DISTAL MEDIAL FEMORAL CON 234703208 DISTAL MEDIAL
• Z-0875-2015 · Dec 4, 2014 · Terminated
  Trilogy Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing pri
• Z-0824-2015 · Nov 21, 2014 · Terminated
  Bone Screw, self-tapping The Trilogy shells are available in three configurations; uni, multi, and cluster-holed. The multi and cluster-holed shells allow for the use of screws to
• Z-2032-2014 · Jun 12, 2014 · Terminated
  Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW, FULLY THREADED, HEX HEAD 4MM DIAMETER, 14 MM LENGTH, and EDI 4.0 MM CANCELLOUS SCREW, FULLY THREADED, 20 MM LENGTH
• Z-1024-2014 · Oct 11, 2013 · Terminated
  TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL 42MM O TRILOGY ACET SHELL 44MM O TRILOGY ACET SHELL 46MM O TRILOGY ACET SHELL 48MM
• Z-0771-2013 · Sep 14, 2012 · Terminated
  Trilogy F/M Acetabular Shell with Uni-Hole. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating h
• Z-0773-2013 · Sep 14, 2012 · Terminated
  Trilogy Acetabular Shell with Cluster Holes. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating
• Z-0772-2013 · Sep 14, 2012 · Terminated
  Trilogy Acetabular Shell Spiked. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating hip damage.
• Z-0775-2013 · Sep 14, 2012 · Terminated
  Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating hip dam
• Z-0769-2013 · Sep 14, 2012 · Terminated
  Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM, 42MM, 44MM, 46MM, 48MM, 50MM, 52MM, 54MM, 56MM, 58MM, 60MM, 62MM, 64MM, 66MM, 68MM, 70MM. The Trilogy Acetabular Sy
• Z-0620-2008 · Oct 19, 2007 · Terminated
  Zimmer Trilogy Acetabular System Shell with Cluster Holes, Porous, 60mm O.D., Tivanium TI-6AL-4V Alloy, Hip Prosthesis Component, REF 6200-060-22, Catalog # 00-6200-060-22, Zimmer

…and 1 more.