Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL) Recalled by Howmedica Osteonics Corp. Due to Ccertain lots of the Restoris MultiCompartmental Knee (MCK)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Howmedica Osteonics Corp. directly.
Affected Products
stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial Knee Arthroplasty surgical procedure
Quantity: 52 units
Why Was This Recalled?
Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking
Where Was This Sold?
U.S., Netherlands, Japan, China, India, Korea, and Australia.
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report