SPORVIEW SELF-CONTAINED STEAM BI SCS-025Recalls & reported problems
SPS Medical Supply Corp. · For use in biologically monitoring all steam sterilizers · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10732224720118), received between Nov 17, 2025 and Nov 17, 2025 — classified as 1 injury.
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 18, 2026.
Reports received per month
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.
InjuryNov 17, 2025Break; Break
CUSTOMER REPORTED NURSE WAS REMOVING THE VIAL FROM THE STERILIZER. WHEN SHE WENT TO CRUSH THE VIAL, IT EXPLODED AND THE VIAL CONTENTS SPLASHED ON TO HER SKIN, GOGGLES, AND CLOTHING, WITH A PIECE OF GLASS HITTING HER CHEEK.
Patient problems: Insufficient Information
MAUDE report 23568889 ↗
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- Bionova® (K)PCD222-CTerragene S.A. · Indicator, Biological Sterilization Process1 recall1 report
- Celerity LCB049Steris Corporation · Indicator, biological sterilization process1 recall1 report
- VERIFY LCB007Steris Corporation · Indicator, biological sterilization process1 recall0 reports
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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