RESTORIS 180702-2Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00848486000837), received between Jun 23, 2021 and Jun 23, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (1 report).

5 other recalls cover devices cleared under the same FDA submission (K082172, K090763, K150307, K220930, K242831); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 23, 2021Positioning Problem; Positioning Problem

  STRYKER REP REPORTED THAT 2 9MM POLYS DID NOT ENGAGE WITH THE TIBIAL BASEPLATE. PROCEDURE COMPLETED BY USING A 10MM.

  Patient problems: Insufficient Information

  MAUDE report 12051550 ↗
• MalfunctionJun 23, 2021Positioning Failure; Positioning Failure

  STRYKER REP REPORTED THAT 2 9MM POLYS DID NOT ENGAGE WITH THE TIBIAL BASEPLATE. PROCEDURE COMPLETED BY USING A 10MM.

  Patient problems: Insufficient Information

  MAUDE report 12051546 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082172, K090763, K150307, K220930, K242831. One submission often covers many models, so check the product and lot details in each record.

• Z-1385-2023 · Mar 10, 2023 · Open, Classified
  stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 5 RM/LL), REF 170615, intended for use in a Partial Knee Arthroplasty surgical procedure
• Z-1386-2023 · Mar 10, 2023 · Open, Classified
  stryker MAKO RESTORIS MCK BASEPLATE TRIAL (SIZE 6 RM/LL), REF 170616, intended for use in a Partial Knee Arthroplasty surgical procedure
• Z-2051-2018 · Jan 19, 2018 · Terminated
  Restoris MCK Onlay Insert Extractor.
• Z-1031-2016 · Jan 15, 2016 · Terminated
  Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee replacement used in conjunction with RIO.
• Z-1132-2014 · Jan 9, 2014 · Terminated
  Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm Interactive Orthopedic System (RIO). It is composed of a unicompartme