CARDINAL HEALTH SAN22ARMMNRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195594554040), received between Jul 6, 2022 and Jul 6, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 6, 2022Material Separation; Material Separation

  CUSTOMER REPORTED LINTING OF THE BLUE COTTON OR TOWELS, PWTB04-STM, FROM THE ARTERIOGRAM PACK, SAN22ARMMN. FIBER, WRAPPED AROUND WIRE WAS VERY DIFFICULT TO REMOVE FROM THE PATIENT. THERE WAS A 10-15 DELAY WITH NO INJURY TO PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14933554 ↗