Centurion SV226UDTRecalls & reported problems
Centurion Medical Products Corporation · SORBAVIEW SHIELD SYS 2.25' X 2.75' ST · Class 1
- 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 20653160253898), received between Jan 16, 2025 and Jan 16, 2025 — classified as 1 injury.
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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 16, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2024 DURING A SEDATED MRI, THE PATIENT HAD A PERIPHERAL IV IN PLACE FOR A SEDATED MRI. THE PERIPHERAL IV WAS DRESSED IN SORBAVIEW SHIELD MICRO BY CENTURION (REF SV226UDT). DURING THE SCAN, THE PATIENT STARTED TO MOVE, HOLD HER BREATH, AND HAVE OXYGEN DESATURATIONS. THE SEDATED MRI TEAM STOPPED THE SCAN AND FOUND THAT THE PATIENT'S IV WAS NO LONGER PATENT DUE TO THE STRUCTURE OF THE DRESSING.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 21170200 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.