GMK Primary Total Knee System 02.07.0110SFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030815928), received between Mar 21, 2019 and Mar 21, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (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 21, 2019Unstable

  PATIENT PRESENTED WITH DISSATISFACTION AND INSTABILITY OF THE KNEE 4 YEARS AND 11 MONTHS AFTER PRIMARY SURGERY. SURGEON WAS CONCERNED AROUND INFECTION, SO HE DECIDED TO REMOVE THE KNEE. INTRA OPERATIVELY HE FOUND OUT THAT INFECTION WAS NEGATIVE. AN HINGE KNEE WAS IMPLANTED.

  Patient problems: Joint Disorder

  MAUDE report 8439900 ↗

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