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Recall Observatory FDA recall evidence

Device product

Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty

Z-3250-2018

August 02, 2018

Class II

Product summary

Firm
Zimmer Biomet, Inc.
Event
Event 80904
Status
Terminated
Classification
Class II
Quantity
16
Official record key
device-enforcement:Z-3250-2018

Official wording

Reason: The implant only has one bolt in the sterile package but it should have had two.

Code information: Lot 585070, UDI (01) 0088030448157 (17) 230215 (10) 585070

Distribution pattern: Worldwide Distribution: US (nationwide) to the following US states: AZ, KS, NM, NV, and UT; and to countries of: Australia and Netherlands.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The implant only has one bolt in the sterile package but it should have had two.