Centurion CIT6610ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653160324096), received between Apr 29, 2024 and Apr 29, 2024 — classified as 1 malfunction.

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.

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.

• MalfunctionApr 29, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ACCORDING TO CUSTOMER, THE "PROVIDER NOTED FLOATING OBJECT INSIDE THE SYRINGE PRIOR TO USE OF INJECTING LIDOCAINE FOR A NEWBORN MALE INFANT. THE SYRINGE IS A 1ML TUBERCULIN SAFETY SYRINGE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19204311 ↗