Skip to content
Recall Observatory FDA recall evidence

Device product

stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial Knee Arthroplasty surgical procedure

Z-1385-2023

March 10, 2023

Class II

Product summary

Firm
Howmedica Osteonics Corp.
Event
Event 91913
Status
Ongoing
Classification
Class II
Quantity
52 units
Official record key
device-enforcement:Z-1385-2023

Official wording

Reason: Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Code information: GTIN 00848486003746, Lot Number 26270421

Distribution pattern: U.S., Netherlands, Japan, China, India, Korea, and Australia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Field note

Send feedback

We'll only use this to respond to your feedback.