CARDINAL HEALTH SNE37BSHNFRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888439124071), received between Mar 23, 2022 and Mar 23, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Jul 14, 2026Class IIOpen, Classified

   Cardinal Health was recently informed of a medical device recall from MEDICOM concerning the Ritmed Neurological Sponges. The recall is being issued due to unexpected variability of endotoxin levels on the products.

   Z-2947-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

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.

• MalfunctionMar 23, 2022Material Separation; Material Separation

  CUSTOMER HAS REPORTED THAT THEY ARE EXPERIENCING LINTING FROM THE OPERATING ROOM TOWELS. CUSTOMER HAS INDICATED THAT THE TOWELS ARE LEAVING LINT ALL OVER THE GLOVES OF THE SURGEON AND ON THE TECHNOLOGISTS. THE BLUE LINT IS ALSO STICKING TO THE PATIENT WHEN CLEANING THEIR SKIN AT THE CONCLUSION OF THE CASE. THERE HAVE BEEN NO INJURIES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13860772 ↗