ClearanceBrief
Recall Z-0737-2023 ยท LOD Bone Cement

Howmedica Osteonics Corp.

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

DateDec 20, 2022 (initiated Nov 7, 2022)
StatusOpen, Classified
ReasonInstructions 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.
Root causeUnder Investigation by firm
ActionUpdate 12/15/22: An UPDATED Urgent Medical Device Correction PFA 3140774 was issued to impacted customers in Turkey only on December 15, 2022. Letter states: 1. Please inform users of this UPDATE Urgent Medical Device Correction and forward this notice to all individuals who need to be made aware. 2. Go to link https://ifu.stryker.com/ and follow instructions for Figures 1 and 2 for the electronic version of the Turkish translated Instructions for Use for affected product outlined in Table 1. 3. Complete and sign the enclosed UPDATE Urgent Medical Device Correction Business Reply Form. Potent
Quantity20 units
DistributionInternational distribution in the country of Turkey.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K014199SURGICAL SIMPLEX P WITH TOBRAMYCIN
Howmedica Osteonics Corp., May 6, 2003