CLOG ZAPPER* with Applicator 120001545Recalls & reported problems
Avanos Medical, Inc. · Enteral Device Declogging System · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00350770456096), received between Jul 23, 2025 and Jul 23, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Leak/Splash” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- Unspecified Eye / Vision Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 23, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED A NURSE HAVING SOME SPLASH IN HER EYE FROM THE CLOG ZAPPER SOLUTION. ADDITIONAL INFORMATION RECEIVED 30-JUN-2025 THE NURSE ATTENDED THE EMERGENCY DEPARTMENT (ED) ON ADVICE FROM THE POISONS INFORMATION CENTRE. THE ADVICE WAS TO GO TO ED AND GET TRIAGED. THE TRAUMA PROVIDER DID A LITMUS TEST WHICH BROUGHT AN ABNORMAL READING. THE TREATMENT IN ED INVOLVED A "LOCAL ANESTHETIC TO BOTH EYES AND AN OSMOTIC IRRIGATION SOLUTION TO DRAW OUT ANY CHEMICALS IN THE EYES UNTIL THE LITMUS READING IS ACCEPTABLE. THEN EYES EXAMINED FOR DAMAGE PLUS FOLLOW-UP APPOINTMENT IN OUTPATIENTS. "THE NURSE WAS WEARING GLASSES BUT WAS LOOKING DOWN WHILE READING THE INSTRUCTIONS TO A SECOND NURSE DOING THE PROCEDURE AND THE SOLUTION SPRAYED INTO THE EYES." NO INJURY WAS SUSTAINED.
Patient problems: Unspecified Eye / Vision Problem
MAUDE report 22579525 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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