Skip to content

POSEY 2791Recalls & reported problems

Posey Products, LLC · POSEY TWICE AS TOUGH CUFF · Class 1

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190676002839), received between Feb 24, 2023 and Feb 24, 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

Device problems

  • Device Slipped1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionFeb 24, 2023Device Slipped; Device Slipped

    THE CUSTOMER REPORTED A COMPLAINT ABOUT PRODUCT 2791. THE CUSTOMER STATED THAT THE RESTRAINTS DO NOT WORK, AND THE PATIENT CAN EASILY GET OUT OF THEM. THE DATE THE ISSUE WAS DISCOVERED IS UNKNOWN, AND NO INJURY WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16440132 ↗

Other Restraint, Protective devices

All Restraint, Protective devices →

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