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POSEY 6027Recalls & reported problems

Posey Products, LLC · BEVELED FLOOR CUSHION · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190676000439), received between May 12, 2023 and May 12, 2023 — classified as 1 injury.

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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Limb Fracture1

Recent adverse event reports

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

  • InjuryMay 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    TIDI RECEIVED A LETTER IN THE MAIL FROM GUST ROSENFELD LAW OFFICE INDICATING THEY RECEIVED A LETTER FROM ANOTHER LAWYER STATING THEIR CLIENT HAD SLIPPED ON A POSEY FALL MAT WHILE VISITING HER SON IN THE HOSPITAL. SHE FRACTURED HER WRIST DUE TO THE FALL. LETTER STATES: SHE CAME IN THE ROOM AND PLACED HER PURSE ON A CHAIR AND THEN TURNED HER BODY, DURING THE PROCESS OF TURNING THE FRONT OF HER FOOT CAUGHT AGAINST THE MAT PLACED ON THE SIDE OF HER SONS BED. SHE ALSO INDICATES LOWER BACK INJURIES.

    Patient problems: Limb Fracture

    MAUDE report 16919564 ↗

Other Bed, Ac-Powered Adjustable Hospital devices

All Bed, Ac-Powered Adjustable Hospital devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.