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Intercept Detergent ML02-0106Recalls & reported problems

Medivators Inc. · Class 1

Adverse event reports
10
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00677964043086), received between Dec 27, 2016 and Apr 21, 2026 — classified as 6 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem3
  • Improper or Incorrect Procedure or Method2
  • Use of Device Problem2
  • Device Operational Issue1
  • Facilities Issue1
  • Leak/Splash1

Patient problems

  • Chemical Exposure9
  • Eye Irritation1
  • Toxicity1

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 21, 2026Leak/Splash

    THE USER FACILITY REPORTED VIA CHEMTREC REPORT THAT AN EMPLOYEE WAS POURING INTERCEPT DETERGENT INTO A SINK WHEN THE PRODUCT SPLASHED PAST THEIR EYE PROTECTION, CAUSING EYE IRRITATION. THE EMPLOYEE IMMEDIATELY FLUSHED THEIR EYES WITH WATER FOR 10-15 MINUTES. THE EMPLOYEE WENT TO BE EVALUATED AT AN OUTPATIENT CENTER; HOWEVER, THEIR SYMPTOMS RESOLVED AND NO ADDITIONAL MEDICAL TREATMENT WAS REQUIRED.

    Patient problems: Eye Irritation

    MAUDE report 24942326 ↗
  • MalfunctionAug 2, 2023Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED VIA CHEMTREC REPORT THAT DURING A PROCEDURE A PATIENT WAS EXPOSED TO INTERCEPT DETERGENT THAT WAS PRESENT ON A GASTROSCOPE THAT HAD NOT BEEN PROPERLY RINSED. NO REPORT OF INJURY OR ADVERSE EFFECTS AND IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.

    Patient problems: Chemical Exposure

    MAUDE report 17444604 ↗
  • InjuryDec 18, 2019Use of Device Problem; Use of Device Problem

    MEDIVATORS RECEIVED AN INCIDENT REPORT FROM CHEMTREC REPORTING THAT A PATIENT EXPERIENCED INTRAVENOUS EXPOSURE TO INTERCEPT DETERGENT. THERE IS POTENTIAL FOR CHEMICAL EXPOSURE SYMPTOMS TO OCCUR.

    Patient problems: Chemical Exposure

    MAUDE report 9489336 ↗
  • InjuryJun 12, 2018Facilities Issue; Facilities Issue

    THE FACILITY REPORTED THAT WHILE AN EMPLOYEE WAS LIFTING INTERCEPT DETERGENT OFF A SHELF, CHEMISTRY FELL AND SPILLED, SPLASHING ONTO HER FACE AND INTO HER EYES.

    Patient problems: Chemical Exposure

    MAUDE report 7594340 ↗
  • InjuryApr 11, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    A FACILITY REPORTED A PATIENT INGESTED INTERCEPT DETERGENT DURING AN ENDOSCOPY PROCEDURE WHEN AN ENDOSCOPE FLUSHED WITH INTERCEPT DETERGENT WAS INSERTED BACK INTO THE PATIENT. THE FACILITY CONTACTED THEIR REGIONAL POISON CONTROL AND CONTINUED TO MONITOR THE PATIENT AFTER THE INCIDENT OCCURRED.

    Patient problems: Chemical Exposure

    MAUDE report 7421627 ↗
  • InjuryMar 19, 2018Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    THE FACILITY REPORTED FOLLOWING A PATIENT ENDOSCOPY PROCEDURE, AN ENDOSCOPE WAS BEING PRECLEANED WITH INTERCEPT DETERGENT WHEN THE PHYSICIAN RETURNED AND INSERTED THE ENDOSCOPE INTO THE PATIENT AGAIN. THE PATIENT WAS EXPOSED TO THE INTERCEPT DETERGENT REMAINING ON THE ENDOSCOPE BEING USED.

    Patient problems: Chemical Exposure

    MAUDE report 7351225 ↗
  • InjuryMay 31, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    FACILITY REPORTED AN EMPLOYEE HAD CHEMICAL EXPOSURE OF INTERCEPT DETERGENT TO THEIR EYE. IT WAS REPORTED THAT THE EMPLOYEE RINSED HIS EYE FOR 15 MINUTES AND SDS WAS SENT TO FACILITY.

    Patient problems: Chemical Exposure

    MAUDE report 6603352 ↗
  • InjuryApr 4, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    FACILITY REPORTED AN EMPLOYEE EXPERIENCE CHEMICAL EYE EXPOSURE TO INTERCEPT DETERGENT.

    Patient problems: Chemical Exposure

    MAUDE report 6458179 ↗
  • Jan 19, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE CASE STATES THAT DURING AN UPPER GI ENDOSCOPY PROCEDURE, A SCOPE MAY HAVE POSSIBLY BEEN FLUSHED WITH INTERCEPT DETERGENT WHILE BEING USED ON A PATIENT. POTENTIAL PATIENT CHEMICAL EXPOSURE.

    Patient problems: Chemical Exposure; Toxicity

    MAUDE report 6264485 ↗
  • Dec 27, 2016Device Operational Issue; Device Operational Issue

    THE CASE STATES THAT A STAFF MEMBER AT FACILITY WAS SPLASHED IN THE EYES WITH INTERCEPT DETERGENT. SHE WAS WEARING GLASSES BUT NOT PROTECTIVE FACE SHIELD. THERE IS POTENTIAL FOR CHEMICAL EXPOSURE SYMPTOMS.

    Patient problems: Chemical Exposure

    MAUDE report 6205164 ↗

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