Jamshidi BEJS4511SPRecalls & reported problems
Carefusion 2200, Inc · Safe-T PLUS Jamshidi Evolve Bone Marrow Biopsy And Aspiration 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 10885403471568), received between Mar 11, 2025 and Mar 11, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Packaging Problem” (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.
Reports received per month
Most reported problems
Device problems
- Packaging Problem1
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.
MalfunctionMar 11, 2025Packaging Problem; Packaging Problem
IT WAS REPORTED THAT PRIOR TO A BONE MARROW PROCEDURE, THE DEVICE TRAY WAS IDENTIFIED DAMAGED RESULTING IN POOR PACKAGE SEAL INTEGRITY. IT WAS FURTHER REPORTED THAT THE DAMAGED TRAY WAS IMMEDIATELY REMOVED FROM THE CASE. THERE WAS NO PATIENT CONTACT. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. RECEIVED TEXT FROM CUSTOMER SURROUNDING DAMAGED CASE OF #BEJS4511. NOTICED DAMAGE TO TRAYS IMMEDIATELY REMOVED FROM CASE IT WAS SHIPPED IN. SAMPLE NOT AVAILABLE. PLEASE SEE ATTACHED PICTURES AND PROVIDE REPLACEMENT 1CA ASAP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21579857 ↗
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- 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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