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TAPER ADAPTOR REMOVAL TOOL 110005232Recalls & reported problems

Biomet Orthopedics, LLC · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304537392), received between May 2, 2023 and May 2, 2023 — classified as 1 malfunction.

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

4 other recalls cover devices cleared under the same FDA submission (K061423, K082996, K093549); 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 2, 2023Fracture; Fracture

    IT WAS REPORTED THAT A PART OF THE MAGNUM TAPER EXTRACTOR BROKE DURING SURGERY. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16852588 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K061423, K082996, K093549. One submission often covers many models, so check the product and lot details in each record.

  • Z-3133-2024 · Aug 8, 2024 · Open, Classified
    Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and acetabular components. Item Number: 650-1
  • Z-3132-2024 · Aug 8, 2024 · Open, Classified
    Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and acetabular components. Item Number: 6
  • Z-0301-2018 · Jun 5, 2017 · Terminated
    CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064
  • Z-0302-2018 · Jun 5, 2017 · Terminated
    CER BIOLOXD OPTION HD 32MM, model # 650-1056

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.