CARDINAL HEALTH ANE4Q8277ARecalls & reported problems
Cardinal Health 200, LLC · KIT,ADULT CSTM ANES CIRCUIT · 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 10197106840856), received between May 30, 2025 and May 30, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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
- Loose or Intermittent Connection1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 30, 2025Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED, THE ADULT ANESTHESIA CIRCUIT DISLODGED FROM THE NECK OF THE CONNECTOR, DURING USE ON THE PATIENT; THE CIRCUIT WAS TAKEN OUT OF USE AND DISCARDED. THERE WAS NO REPORTED INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22119553 ↗
Other TRAY, SURGICAL devices
- Centurion MNS11625Centurion Medical Products Corporation · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDA2526Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1470BMedline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1534Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYKM1790AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- Centurion ART245ACenturion Medical Products Corporation · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYNDC1786AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE ART970Medline Industries, Inc. · TRAY, SURGICAL2 recalls0 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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