Jamshidi BEJS4511Recalls & reported problems
Carefusion 2200, Inc · Jamshidi Evolve Bone Marrow Biopsy Tray - 11G x 4" EJ Biopsy/Aspiration Needle, Specimen Cradle and 15G TJ Aspiration Needle (Adjustable Length) · Class 2
All models of Jamshidi (18)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403471582), received between Apr 6, 2022 and Apr 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 16, 2026.
Most reported problems
Device problems
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2022Material Separation; Material Separation
IT WAS REPORTED THAT A COMPONENT DISCONNECTED FROM BIOPSY NEEDLE. VERBATIM: TODAY ONE OF OUR PROVIDERS WAS PERFORMING A BONE MARROW BIOPSY AND THE WHITE CAP ATTACHED TO THE TOP OF THE BONE MARROW CRADLE POPPED UP TOTALLY. IT WAS NOT LONGER ATTACHED TO THE DEVICE. LUCKILY THE PROVIDER WAS ABLE TO REMOVE THE CRADLE WITH A PAIR OF KELLY CLAMPS AND THE CORE WAS ALSO RETRIEVED. THE LOT # FOR THIS KIT IS 0001432964 WITH AN EXPIRATION DATE OF 08/31/2022. WHAT WAS THE IMPACT TO THE PATIENT? WAS THEY ABLE TO COMPLETE THE PROCEDURE SUCCESSFULLY? THROUGH XXXX EXPERTISE HE WAS ABLE TO SUCCESSFULLY COMPLETE THE PROCEDURE USING A PAIR OF KELLY CLAMPS TO EXTRACT THE BROKEN BONE MARROW CRADLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14021589 ↗
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- MAX-CORE MC1820Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall2,404 reports
- MAX-CORE MC1816Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall1 death848 reports
- MAX-CORE MC1410Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall399 reports
- MAX-CORE MC1610Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall394 reports
- ENCOR® ECP0110GVSenorx, Inc. · INSTRUMENT, BIOPSY392 reports
- ENCOR® ECP0110GSenorx, Inc. · INSTRUMENT, BIOPSY390 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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