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Recall Observatory FDA recall evidence

Device product

Tobra Full Dose CE Antibiotic Simplex P- Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number:6197-1-001

Z-0737-2023

November 07, 2022

Class III

Product summary

Firm
Howmedica Osteonics Corp.
Event
Event 91147
Status
Ongoing
Classification
Class III
Quantity
20 units
Official record key
device-enforcement:Z-0737-2023

Official wording

Reason: Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is accurate.

Code information: UDI# P/N 6197-1-001 (01)07613327128741 (17)230331(10)lot# GTIN: 07613327128741-Instructions for Use (IFU) received with product: 0700-7-012 (IFU Radiopaque Bone Cement) All lots manufactured under Rev AB, which with expiration date on/after October 28, 2021

Distribution pattern: International distribution in the country of Turkey.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is accurate.