Foreign Body Retrieval Hood Protector 92810Recalls & reported problems
Avanos Medical, Inc. · Foreign Body Retrieval Hood Protector · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00350770928104), received between Sep 20, 2019 and Nov 5, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component2
Patient problems
- Foreign Body In Patient1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 5, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED "WHEN USING THE PROTECTIVE CAP ON THE ENDOSCOPE, IT BROKE OFF... THE PROTECTIVE CAP BROKE INSIDE THE PATIENT." ADDITIONAL INFORMATION RECEIVED 13-OCT-2025 STATING "PATIENT UNINJURED. NO FURTHER MEDICAL INTERVENTION REQUIRED. PATIENT DISCHARGED WITHOUT COMPLICATIONS."
Patient problems: Foreign Body In Patient
MAUDE report 23480448 ↗MalfunctionSep 20, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED "THE FOREIGN BODY HOOD RETRIEVER CAME OFF OF THE SCOPE & LODGED IN THE [PATIENT'S] CRICOPHARYNGEUS". THERE WAS NO REPORTED INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9098095 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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