Jamshidi EJC4008Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403464058), received between May 8, 2026 and May 8, 2026 — classified as 1 malfunction.

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 16, 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.

• MalfunctionMay 8, 2026Contamination

  IT WAS REPORTED BY THE CUSTOMER THAT DURING A JAMSHIDI BONE MARROW BIOPSY PROCEDURE, AFTER EJECTING THE CORE FROM THE CANNULA, THE PHYSICIAN NOTICED THAT A SMALL PIECE OF METAL CAME OUT BEHIND IT. NO PATIENT HARM WAS REPORTED. DURING FOLLOW UP RESPONSE IT WAS FURTHER REPORTED THAT A METAL FRAGMENT MEASURING LESS THAN 1 CM WITH A ROUNDED SHAPE WAS OBSERVED. THERE WAS NO REPORTED IMPACT TO THE PATIENT, HEALTHCARE PROVIDER, USER, OR OTHERS, AND NO MEDICAL INTERVENTION, DIAGNOSTICS, PROCEDURES, OR TREATMENT DELAYS WERE REQUIRED. THE JAMSHIDI NEEDLE WAS USED IN ACCORDANCE WITH THE INSTRUCTIONS FOR USE (IFU), AND NO DIFFICULTY OR RESISTANCE WAS NOTED DURING USE OF THE DEVICE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25131149 ↗