GMK Primary Total Knee System 02.07.2205RRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030820878), received between Mar 29, 2019 and Mar 29, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (1 report).

1 other recall cover devices cleared under the same FDA submission (K090988); 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 29, 2019Loose or Intermittent Connection

  ON FEBRUARY 28 2019 WE WERE INFORMED ABOUT A REVISION SURGERY PERFORMED ON (B)(6), 4 YEARS AND 9 MONTHS AFTER PRIMARY SURGERY, DUE TO AN INFECTION (4 TO 5 MULTIRESISTANT GERMINATIONS: STREPTOCOCCUS). DURING SURGERY, THE SURGEON TOOK THE LINER OUT AND NOTICED THE TIBIA IMPLANT IS LOOSE. IT WAS NOT FORESEEABLE ON THE X-RAYS AND THE PATIENT HAS NO PAIN BECAUSE HIS TOES HAVE BEEN AMPUTATED AND HE IS IN A WHEELCHAIR.

  Patient problems: Unspecified Infection

  MAUDE report 8464673 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K090988. One submission often covers many models, so check the product and lot details in each record.

• Z-0266-2018 · Oct 24, 2017 · Terminated
  The GMK knee system: designed for cemented use in total knee arthroplasty. Sphere and Primary Inserts with part number ranges: 02.12.0110FL - 02.12.0620FL; 02.12.0110FR - 02.12.0