Halyard RCDI27-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10809160481073), received between Aug 6, 2026 and Aug 6, 2026 — classified as 1 injury.

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

• InjuryAug 6, 2026Contamination

  It was reported that, while preparing to drape the patient, the certified surgical technologist identified a hair inside the folded large drape. As a precaution, additional pre-incision antibiotics were administered to the patient. The surgeon paused the procedure to determine the appropriate course of action, resulting in an approximate 15-minute delay to the surgery.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 50158093 ↗