Steelco ID 300/2Recalls & reported problems
Steelco SPA · This device drying cabinet provides fast drying of instruments, equipment and general item. Items are stored in controlled environment. · 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 08051520012693), received between Dec 29, 2025 and Dec 29, 2025 — classified as 1 malfunction.
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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Keratitis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 29, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
WHILE TROUBLESHOOTING AN ID 300/2 DRYING CABINET THAT DISPLAYED AN ERROR RELATED TO THE UV LAMP, THE TECHNICIAN REMOVED THE BPA FILTER TO CHECK IF ALL THREE LAMPS WERE FUNCTIONING. THE TECHNICIAN OBSERVED THE LAMPS FOR LESS THAN FIVE SECONDS ON THREE SEPARATE OCCASIONS BEFORE CLOSING THE SYSTEM. EXPOSURE TO THE UV LIGHT, EVEN FOR THESE BRIEF MOMENTS, RESULTED IN MILD PHOTOKERATITIS (A SENSATION SIMILAR TO HAVING SAND IN THE EYES). THE IRRITATION WAS TEMPORARY, WITH NO PERMANENT DAMAGE, AND VISION RETURNED TO NORMAL. ACCORDING TO THE DOCTOR'S NOTE, THE TECHNICIAN WAS CLEARED TO RETURN TO WORK THE SAME DAY. NO PATIENTS WERE INVOLVED IN THIS INCIDENT.
Patient problems: Keratitis
MAUDE report 23907476 ↗
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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