POSEY 2700QLRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10190676002808), received between Dec 7, 2022 and Jan 29, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Break” (4 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 29, 2026Break

  SUPPLEMENTAL MEDWATCH BEING SENT FOR ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24209903 ↗
• MalfunctionDec 8, 2023Break; Break

  ADDITIONAL PRODUCT RETURNED. THE CUSTOMER IS STATING THAT PATIENTS ARE RIPPING THROUGH THE THIN PART OF THE MATERIAL. THE STAFF DID NOT WITNESS HOW IT HAPPENED AND IT WAS DISCOVERED DURING 15 MIN SAFETY CHECK.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18297439 ↗
• MalfunctionApr 20, 2023Break; Break

  CUSTOMER IS REPORTING A COMPLAINTS ABOUT (B)(4)CUSTOMER STATES THAT WHILE THE (B)(4) WAS IN USE ONE OF THE PRONGS ON THE MALE SIDE OF THE BUCKLE BROKE. THIS ALLOWED THE PATIENT TO GET FREE OF THE RESTRAINTS. THERE ARE NO REPORTED INJURIES AS A RESULT. CUSTOMER HAS PRODUCT AVAILABLE TO SEND IN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16774027 ↗
• MalfunctionDec 7, 2022Break; Break

  CUSTOMER IS GOING TO RETURN PRODUCT # 2700QL DUE TO COMPLAINT. CUSTOMER STATED PATIENT BROKE OUT OF TAT RESTRAINTS DUE TO BROKEN BUCKLE. NO EXPLANATION ON HOW THE BUCKLE BROKE. PRODUCT # 2700QL WITH LOT# 1288T070.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15932428 ↗