Moray 00711889Recalls & reported problems
US Endoscopy · The Moray micro forceps is designed to enhance sampling from lesions that can occur within and outside of the gastrointestinal tract. · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995184094), received between Mar 25, 2021 and Mar 28, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Difficult to Open or Close” (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
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Difficult to Open or Close1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Pancreatitis1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 28, 2025Difficult to Open or Close; Insufficient Device Problem Information; Difficult to Open or Close; Insufficient Device Problem Information
THE USER FACILITY REPORTED VIA VIGILANCE REPORT ((B)(4)), THAT DURING A PATIENT PROCEDURE, THEIR MORAY FORCEPS DID NOT OPEN WHEN THE HANDLE WAS OPENED. NO CONTACT WITH THE PATIENT AND NO PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21720305 ↗InjuryMar 25, 2021Adverse Event Without Identified Device or Use Problem
THE DISTRIBUTOR REPORTED THAT A PATIENT DEVELOPED PANCREATITIS FOLLOWING A PROCEDURE WHICH INCLUDED USE OF THE MORAY MICRO FORCEPS THROUGH A 19G FNA NEEDLE FOR SAMPLING A PANCREATIC CYST. THE USER OF THE DEVICE HAS DECLINED TO PROVIDE PATIENT STATUS OR TREATMENT INFORMATION BEYOND THE DEVELOPMENT ON PANCREATITIS.
Patient problems: Pancreatitis
MAUDE report 11571051 ↗
Other FORCEPS, BIOPSY, NON-ELECTRIC devices
- Radial Jaw 4 M00513410Boston Scientific Corporation · FORCEPS, BIOPSY, NON-ELECTRIC1 recall24 reports
- Radial Jaw 4 M00513330Boston Scientific Corporation · FORCEPS, BIOPSY, NON-ELECTRIC1 recall19 reports
- Radial Jaw 4 M00513400Boston Scientific Corporation · FORCEPS, BIOPSY, NON-ELECTRIC1 recall16 reports
- NA 8736685Richard Wolf GmbH · FORCEPS, BIOPSY, NON-ELECTRIC1 recall15 reports
- NA 828051Richard Wolf GmbH · FORCEPS, BIOPSY, NON-ELECTRIC1 recall6 reports
- Radial Jaw 4 M00513320Boston Scientific Corporation · FORCEPS, BIOPSY, NON-ELECTRIC1 recall3 reports
- Radial Jaw 4 M00513360Boston Scientific Corporation · FORCEPS, BIOPSY, NON-ELECTRIC1 recall2 reports
- NA 8735685Richard Wolf GmbH · FORCEPS, BIOPSY, NON-ELECTRIC1 recall1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.