Skip to content
Recall Observatory FDA recall evidence

Device product

BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORAL CERAMIC 28MM +0 19025 HEAD FEMORAL CERAMIC 32MM -3 19026 HEAD FEMORAL CERAMIC 32MM +0 19027 HEAD FEMORAL CERAMIC 32MM +3

Z-0151-2026

September 09, 2025

Class II

Product summary

Firm
BioPro, Inc.
Event
Event 97605
Status
Ongoing
Classification
Class II
Quantity
147 total
Official record key
device-enforcement:Z-0151-2026

Official wording

Reason: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Code information: Product ID/UDI-DI 19023 M20919023 19024 M20919024 19025 M20919025 19026 M20919026 19027 M20919027 All lots, all serial numbers

Distribution pattern: US Domestic distribution to Texas and Michigan.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    packaging issue
  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    loss of sterility