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JAMSHIDI SN1015XRecalls & reported problems

Carefusion 2200, Inc · JAMSHIDI NEEDLE BIOPSY 15G X 100MM DISP · Class 1

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 10885403076152), received between May 20, 2022 and May 20, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Contamination with Chemical or Other Material1

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.

  • MalfunctionMay 20, 2022Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

    IT WAS REPORTED THAT CUSTOMER RECEIVED STERILE PRODUCT THAT HAS BEEN SEALED WITH A STRAND OF HUMAN HAIR. VERBATIM: ALSO, WE RECEIVED STERILE PRODUCT THAT HAS BEEN SEALED WITH A STRAND OF HUMAN HAIR. REF (B)(4), LOT 0001224605.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14454703 ↗

Other Tray, surgical, needle devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.