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Recall Observatory FDA recall evidence

Device product

Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 56mm, O.D. (Acetabular Cup), Catalog Number 140-01-56; For use in primary total hip arthroplasty.

Z-1901-2016

April 12, 2016

Class II

Product summary

Firm
Exactech, Inc.
Event
Event 73200
Status
Terminated
Classification
Class II
Quantity
2 devices.
Official record key
device-enforcement:Z-1901-2016

Official wording

Reason: Devices were inadvertently sent to packaging and finished goods prior to the PMA site-change supplement approval.

Code information: Product Code: MRA, Catalog Number 140-01-56, Serial Numbers: 4268399 and 4268400, Exp. 2/6/2021.

Distribution pattern: Distributed in FL, NJ, NY, OH, OK, RI, TN, VA and HI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Devices were inadvertently sent to packaging and finished goods prior to the PMA site-change supplement approval.