AquaGuard 50015-RPKRecalls & reported problems
Tidi Products, LLC · TIDI Moisture Barrier Clear Polyethylene 5 per Package · Class 1
Data updated Oct 18, 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 00618125190294), received between Dec 26, 2024 and Dec 26, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Moisture Damage” (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
- Moisture Damage1
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.
MalfunctionDec 26, 2024Moisture Damage; Moisture Damage
AGAIN I HAVE TO UNFORTUNATELY USE YOUR PRODUCT AGAIN AND THIS IS THE RESULT FROM IT. I NOW HAVE TO GET THE IR TEAM TO COME STICK ME AGAIN WHICH IS JUST A GREAT TIME AND ALL BECAUSE OF YOUR POOR QUALITY PRODUCT. WHAT ARE YOU PEOPLE THINKING OVER THERE?? HOW DO YOU PEOPLE EVEN STAY IN BUSINESS AND WHY IS THERE NO COMPETITION TO YOU?
Patient problems: Insufficient Information
MAUDE report 21020400 ↗
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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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