POSEY 6027RRecalls & reported problems

Posey Products, LLC · REFLECTIVE BEVEL CUSHION · Class 2

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 10190676000873), received between Jul 9, 2024 and Jul 9, 2024 — 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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

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.

MalfunctionJul 9, 2024Device Slipped; Device Slipped
CUSTOMER REPORTED COMPLAINT REGARDING PRODUCT PART 6027R SLIDING ON THE FLOOR. THE DATE THE ISSUE WAS DISCOVERED IS UNKNOWN AND NO PATIENT INCIDENT OR INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19702833 ↗

Device details

UDI-DI	`10190676000873`
Brand	POSEY
Model	6027R
Company	Posey Products, LLC
Product code	FNL · Bed, Ac-Powered Adjustable Hospital
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Nov 15, 2022

Device type (GMDN): Floor covering

A material intended to be used to cover the floor of a room where certain consideration must be taken to the degree of safety and/or hygiene required. It is typically used as a non-slip surface, a water-resistant surface, and/or an industrial surface in areas such as examination rooms or operating rooms; it may be conductive, to reduce the risk of static electricity, or non-conductive.

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