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POSEY 2750Recalls & reported problems

Posey Products, LLC · POSEY TAT FOR STRETCHER · 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 10190676002815), received between Oct 7, 2022 and Oct 7, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Disconnection” (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

  • Disconnection1

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.

  • MalfunctionOct 7, 2022Disconnection; Disconnection

    CUSTOMER REPORTED VIA EMAIL THAT THEY HAD A PATIENT WHO WAS BEING TRANSPORTED VIA AMBULANCE. HE WAS BEING COMBATIVE PSYCHIATRIC PATIENT DURING TRANSPORT. THE POSEY RESTRAINTS WERE APPLIED TO THE PATIENT'S WRIST AND ANKLES TO PHYSICALLY RESTRAIN THE PATIENT. THE PATIENT WAS ABLE TO START PULLING THE VELCRO OFF ONE OF THEIR RESTRAINTS. HE WAS ABLE TO GET OUT OF RESTRAINT, PULLED OFF THE SPIT HOOD, AND SPAT AT EMPLOYEE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15562238 ↗

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.