POSEY 2792QRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190676003614), received between Sep 9, 2022 and Nov 8, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 8, 2022Break; Break

  SUPPLEMENTAL MEDWATCH REQUIRED FOR ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15754285 ↗
• MalfunctionSep 9, 2022Material Split, Cut or Torn; Material Split, Cut or Torn

  THE CUSTOMER CONTACTED US VIA E-MAIL STATING THAT THEY HAVE A 2793 RESTRAINT THAT RIPPED AT THE SEAMS. THE PATIENT WAS ACTIVE/COMBATIVE. THE CUSTOMER STATES THIS IS THE 2ND PAIR THAT TORE AT THE SEEMS. CUSTOMER STATES THEY HAVE THE ORIGINAL PRODUCT TO RETURN. NO LOT# OR GTIN INFORMATION WAS AVAILABLE. ONLY A SINGLE 2793 RESTRAINT WAS RECEIVED ON AUGUST 26TH, BUT ADDITIONAL PRODUCT WAS RECEIVED WITH A PART NUMBER: 2792Q LEADING TO GENERATE THIS MEDWATCH.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15396272 ↗