Jamshidi TJC4008Recalls & reported problems
Carefusion 2200, Inc · JAMSHIDI (TJ) BONE MARROW BIOPSY/ASPIRATION NEEDLE 8G X4 · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403044038), received between Mar 15, 2022 and Mar 15, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Complete Blockage” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Jun 23, 2021Open, Classified
Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
Z-2247-2021 · Root cause: Packaging process control · FDA record ↗
Most reported problems
Device problems
- Complete Blockage1
Patient problems
- Needle Stick/Puncture1
- 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.
InjuryMar 15, 2022Complete Blockage; Complete Blockage
IT WAS REPORTED "CONCERNING THE BONE MARROW PUNCTURE NEEDLE, JAMSHIDI REG TJC4008 LOT 0001435436 2026-09-30, THE DIABOLO TO GUIDE THE NEEDLE IN THE RIGHT DIRECTION IS BLOCKED. 2 CASES WERE NOTED BY THE HEMATOLOGIST; 1 DEFECTIVE PART IS IN THE PHARMACY". CONCERNING THE BONE MARROW PUNCTURE NEEDLE, JAMSHIDI REG TJC4008 LOT 0001435436 2026-09-30, THE DIABOLO ALLOWING TO GUIDE THE NEEDLE IN THE RIGHT DIRECTION IS BLOCKED. 2 CASES WERE NOTED BY THE HEMATOLOGIST WHO PRICKED HERSELF FOLLOWING THIS PROBLEM; 1 DEFECTIVE PART IS IN THE PHARMACY. WAS THERE A NEED FOR MEDICAL INTERVENTION DUE TO WHAT HAPPENED (ADMINISTRATION OF MEDICATIONS, ETC)? (DETAIL) - NO IS THERE A PHOTO OR SAMPLE AVAILABLE SHOWING THE REPORTED ISSUE? - SAMPLE AVAILABLE. I HAVE THEM AT HOME.
Patient problems: Needle Stick/Puncture; No Clinical Signs, Symptoms or Conditions
MAUDE report 13770517 ↗
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- 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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