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Recall Observatory FDA recall evidence

Device product

OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: OmniPore Surgical Implants in block, sheet, and anatomical shapes are intended for nonweight bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. OmniPore Surgical Implants are also intended for the augmentation or restoration of contour in the craniomaxillofacial skeleton.

Z-1224-2019

January 30, 2019

Class II

Product summary

Firm
Matrix Surgical Holdings, LLC
Event
Event 82487
Status
Terminated
Classification
Class II
Quantity
42
Official record key
device-enforcement:Z-1224-2019

Official wording

Reason: Product mislabeling.

Code information: OP9520 / Lot # 00855421005871 022050617

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of Florida and Massachusetts and countries of Argentina, Chile, Colombia, Iran, Mexico, Norway, Taiwan, and Turkey.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    mislabeling