ENDODRY Storage and Drying CabinetRecalls & reported problems
Cantel Medical (Italy) Srl · ENDODRY one-click Storage and Drying System is an endoscope storage cabinet with directed airflow, which aids in drying, for storing flexible endoscopes which have been previously cleaned and high-level disinfected in a validated reprocessor. One site Opening operator site left. · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 18011517151207), received between Jul 27, 2026 and Aug 14, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 14, 2026Insufficient Device Problem Information
The user facility reported that they are observing damage to their scopes after being stored in their Endodry Storage and Drying System. One of these scopes was later used in a patient procedure, and a colonic hematoma was reported.
Patient problems: Insufficient Information
MAUDE report 50251933 ↗MalfunctionJul 27, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50014211 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.