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Trabecular Metal® 00-4349-036-06 (UDI 00889024633070)Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of Trabecular Metal (74)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024633070), received between Jun 9, 2022 and Jul 1, 2024 — classified as 2 injuries.

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

14 other recalls cover devices cleared under the same FDA submission (K052906, K130661); 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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 1 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Device Dislodged or Dislocated2
  • Unstable1

Patient problems

  • Joint Dislocation1
  • Loss of Range of Motion1
  • No Clinical Signs, Symptoms or Conditions1
  • Pain1

Recent adverse event reports

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

  • InjuryJul 1, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED THAT THE PATIENT HAD INITIAL SURGERY APPROXIMATELY 2 YEARS AGO. SUBSEQUENTLY, THE PATIENT EXPERIENCED PAIN AND RANGE OF MOTION ISSUES AFTER PULLING A CANOE OUT OF THE WATER, WHICH CAUSED DISLOCATION. THE PATIENT WAS REVISED APPROXIMATELY 3 WEEKS AGO.

    Patient problems: Joint Dislocation; Loss of Range of Motion; Pain

    MAUDE report 19643334 ↗
  • InjuryJun 9, 2022Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

    IT WAS REPORTED THAT THE PATIENT HAD A COMPETITOR ANATOMIC SHOULDER REVISION. SUBSEQUENTLY, THE PATIENT REVISED THE HUMERAL SIDE AGAIN AS SHE SUBLUXED POST-SURGERY AND WAS UNSTABLE. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14643322 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K052906, K130661. One submission often covers many models, so check the product and lot details in each record.

  • Z-0299-2020 · Oct 10, 2019 · Terminated
    Trabecular Metal Reverse Shoulder System, Item Nos. 00434210613 00430900103 00434210613 00434210813 00434210817 00434210913 00434211013 00434211017 00434211113 00434211213 00434211
  • Z-3144-2017 · May 22, 2017 · Terminated
    Zimmer Trabecular Metal Reverse Shoulder System Instrumentation, Drill 2.5 mm Diameter, Item Number/EDI 47430904601, Sterile
  • Z-0609-2014 · Dec 10, 2013 · Terminated
    Trabecular Metal (TM) Reverse Glenosphere 36mm Part 00-4349-036-11 The reverse shoulder system is used in the treatment of the following: severe pain or significant disability in
  • Z-1079-2014 · Oct 17, 2013 · Terminated
    Trabecular Metal" Reverse Shoulder System
  • Z-2055-2013 · Aug 1, 2013 · Terminated
    00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx, Non sterile (sterilize before use) The Glenosphere Distractor must be able to attach, connect, or mate
  • Z-0574-2011 · Sep 10, 2010 · Terminated
    Zimmer Trabecular Metal Humeral Stem Surgical Technique. Catalog Number: 97-4309-002-00, Rev. 3 The Zimmer Trabecular Metal Shoulder System consists of conventional and reverse, s
  • Z-0576-2011 · Sep 10, 2010 · Terminated
    Zimmer Trabecular Metal Reverse Shoulder System Surgical Technique. Catalog Number 97-4309-003-00, Rev. 4. The Zimmer Trabecular Metal Reverse Shoulder System is a treatment option
  • Z-0570-2011 · Sep 10, 2010 · Terminated
    ZIMMER TRABECULAR METAL SHOULDER INSTRUMENTATION, DISTAL PILOT used for implantation of the Zimmer Trabecular Metal Humeral and/or Zimmer Trabecular Metal Reverse Shoulder Systems:
  • Z-0573-2011 · Sep 10, 2010 · Terminated
    TRABECULAR METAL" SHOULDER REAMER CASE used for implantation of the Zimmer Trabecular Metal Humeral and/or Zimmer Trabecular Metal Reverse Shoulder Systems: Catalog Number 00-4312-
  • Z-0575-2011 · Sep 10, 2010 · Terminated
    Zimmer Trabecular Metal Humeral Stem 4-Part Fracture Surgical Technique. Catalog Number 97-4309-004-00, Rev. 3. The Zimmer Trabecular Metal Shoulder System consists of convention
  • Z-0571-2011 · Sep 10, 2010 · Terminated
    ZIMMER TRABECULAR METAL" SHOULDER INSTRUMENTATION, DISTAL PILOT used for implantation of the Zimmer Trabecular Metal Humeral and/or Zimmer Trabecular Metal Reverse Shoulder Systems
  • Z-1417-06 · Jul 20, 2006 · Terminated
    Zimmer Trabecular Metal Reverse Shoulder System Glenosphere, 40 mm diameter; Catalog/Ref No. 00-4349-040-01.
  • Z-1418-06 · Jul 20, 2006 · Terminated
    Zimmer Trabecular Metal Reverse Shoulder System Base Plate; Catalog/Ref No. 00-4349-038-00.
  • Z-1416-06 · Jul 20, 2006 · Terminated
    Zimmer Trabecular Metal Reverse Shoulder System Glenosphere, 36 mm diameter; Catalog/Ref No. 00-4349-036-01.

Other PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED devices

All PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED devices →

Sources and updates

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