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Recall Observatory FDA recall evidence

Device product

TunneLoc Tibial Fixation Device Product Usage: To provide fixation of soft tissue grafts within the tibial tunnel during anterior cruciate ligament (ACL) and/or posterior cruciate ligament (PCL) reconstruction.

Z-1071-2018

October 11, 2017

Class II

Product summary

Firm
Zimmer Biomet, Inc.
Event
Event 79263
Status
Terminated
Classification
Class II
Quantity
14,461
Official record key
device-enforcement:Z-1071-2018

Official wording

Reason: Gamma sterilization validation testing indicates the sterilization dose for the product may not be adequate.

Code information: 906512, 906513, 906514, 906515

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Gamma sterilization validation testing indicates the sterilization dose for the product may not be adequate.