Jamshidi DIN1518XRecalls & reported problems
Carefusion 2200, Inc · ILLINOIS NEEDLE BONE MARROW 18G ADJUSTABLE LEN · Class 2
All models of Jamshidi (18)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885403087073), received between Mar 4, 2022 and Oct 12, 2023 — classified as 3 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Contamination1
- Crack1
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 12, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT, USER FOUND THERE WAS NO PRODUCT INFORMATION LABEL ON THE ACTUAL GOODS INSIDE THE BOX. IT WAS REPORTED THAT, THE USER SUSPECTS NEEDLE CRACK DURING USE. IT WAS OBSERVED AIR LEAKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17923125 ↗MalfunctionOct 12, 2023Crack; Crack
IT WAS REPORTED THAT, USER FOUND THERE WAS NO PRODUCT INFORMATION LABEL ON THE ACTUAL GOODS INSIDE THE BOX. IT WAS REPORTED THAT, THE USER SUSPECTS NEEDLE CRACK DURING USE. IT WAS OBSERVED AIR LEAKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17923123 ↗MalfunctionMar 4, 2022Contamination; Contamination
WHERE DURING THE CONTROL A BLUE PLASTIC DEBRIS WAS NOTICED. HE OBSERVED THE PRESENCE OF "BLUE" COLORED PARTICLES (INSIDE THE INDIVIDUAL PACKAGING) WHICH WOULD APPEAR TO BE "DEBRIS" OF BLUE PLASTIC FROM THE DEVICE. THE MANUFACTURER IS REQUIRED TO JUSTIFY THE PRESENCE AND HARMLESSNESS OF THESE "DEBRIS".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13670307 ↗
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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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