ClearanceBrief
Recall Z-0999-2024 ยท LXH Orthopedic Manual Surgical Instrument

Howmedica Osteonics Corp.

HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty

DateFeb 6, 2024 (initiated Dec 22, 2023)
StatusOpen, Classified
ReasonFailed to meet the acceptance criteria for the seal integrity and/or package integrity testing for the Sterile Barrier Outer Pouch and the Protective Barrier Inner Pouch, compromising product sterility
Root causePackage design/selection
ActionStryker issued Urgent Medical Device Recall (UMDR) PFA 3285098 was issued by third party Sedgwick on 22/DEC/2023 via UPS 2-day air. OUS customer notification will be issued at the country level. Letter states reason for recall, health risk and action to take: 1. Please inform users of this Urgent Medical Device Correction and forward this notice to all individuals who need to be made aware. 2. Immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility. 3. Dispose of all affected products listed in the Part an
DistributionWorldwide distribution - US Nationwide and the countries of Argentina, Australia, Brazil, Canada, Chile, China (Hong Kong), Columbia, Italy, Japan, Malaysia, Netherlands (Venlo), Slovenia, S. Africa, Spain, Sweden, Switzerland, Thailand, United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.