POSEY 6026Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190676000422), received between Jan 16, 2023 and Jan 16, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Slipped” (1 report).

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

• MalfunctionJan 16, 2023Device Slipped; Device Slipped

  CUSTOMER REPORTS AN ISSUE WITH 6026 FLOOR CUSHION. CUSTOMER STATES THAT THEY PURCHASED QTY 32 OF THE 6026 IN JULY. THEY STATE AFTER 5 MONTHS OF USE THE MATS HAVE BECOME SLIPPERY UNDERNEATH AND OR WILL GLIDE/MOVE ON THE FLOOR WHICH COULD CAUSE A POTENTIALLY DANGEROUS SITUATION FOR THE STAFF AND PATIENTS. NO REPORTED INCIDENTS AS OF YET.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16174609 ↗