Advantage™ Saliva Ejectors ZWWIRecalls & reported problems
Crosstex International, Inc. · Saliva Ejectors, White, White · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10732224000739), received between May 25, 2023 and May 25, 2023 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 25, 2023Break; Break
THE USER FACILITY REPORTED VIA USER FACILITY MEDWATCH REPORT # MW5117102 THAT DURING FIVE DIFFERENT DENTAL PROCEDURES THE TIP OF THEIR ADVANTAGE SALIVA EJECTOR BROKE OFF. IN TWO CASES, THE TIP DETACHED AND WAS SWALLOWED BY THE PATIENT. THESE PATIENTS WERE ADVISED BY THE USER FACILITY TO SEEK MEDICAL ATTENTION AND LET THE FACILITY KNOW IF THERE WERE ANY ISSUES. IN THE REMAINING THREE CASES, THE TIP DETACHED AND ALL COMPONENTS WERE SUCCESSFULLY RETRIEVED FROM THE PATIENT'S MOUTH. THERE WAS NO REPORT OF INJURY FOR ANY OF THE CASES.
Patient problems: Insufficient Information
MAUDE report 17008318 ↗
Other Mouthpiece, saliva ejector devices
- Argyle 8881450004Cardinal Health, Inc. · Mouthpiece, saliva ejector9 reports
- Comfort Plus™ Premium Saliva Ejectors ZWWCPCrosstex International, Inc. · Mouthpiece, saliva ejector2 reports
- MEDICOM SAFEBASICS 700AMD Medicom Inc · Mouthpiece, saliva ejector1 report
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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