Foreign Body Retrieval Basket 92766Recalls & reported problems

Avanos Medical, Inc. · Foreign Body Retrieval Basket · 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 00350770927664), received between Sep 17, 2024 and Sep 17, 2024 — classified as 1 malfunction.

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. 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

Break1

Patient problems

Foreign Body In Patient1

Recent adverse event reports

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

MalfunctionSep 17, 2024Break; Break
IT WAS REPORTED THE CLINICIANS "USED A FOREIGN BODY RETRIEVAL BASKET DURING A BRONCHOSCOPY PROCEDURE. WHEN PUSHED THROUGH THE SCOPE, THE ROUND TIP OF THE BASKET CAME OFF IN THE PATIENT'S LUNG." ADDITIONAL INFORMATION RECEIVED 21-AUG-2024 STATED THIS HAPPENED "DURING A BRONCHOSCOPY WHILE TRYING TO RETRIEVE [A] FOREIGN BODY." THE PATIENT WAS TRANSFERRED TO A TERTIARY FACILITY. THE DEVICE FELL INTO THE PATIENT'S LEFT LUNG.
Patient problems: Foreign Body In Patient
MAUDE report 20237714 ↗

Device details

UDI-DI	`00350770927664`
Brand	Foreign Body Retrieval Basket
Model	92766
Catalog no.	60718
Company	Avanos Medical, Inc.
Product code	FDX · endoscopic cytology brush
Class	Class 2
FDA submission	K941464
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 22, 2023

Device type (GMDN): Rigid endoscopic stone-retrieval forceps, reusable

A rigid manual device intended to be inserted through the working channel of a compatible endoscope to grasp and remove stones (e.g., calculi from the urinary tract) or foreign bodies during an endoscopic procedure. It is typically a very long instrument with one sliding and one stationary rod, or a sheath, whose distal ends are equipped with thin grasping claws in which the stone is seized and held for extraction. The claws are typically operated by scissors-like ring handles at the proximal end of the instrument. This is a reusable device.

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