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Jamshidi

CAREFUSION 2200, INC · Model BAT3018 · UDI-DI 10885403107603

LWEFMI Prescription
3
510(k) clearances
46
Adverse events
1
Recalls
21
Facilities

Description

ILLINOIS (TIN) BONE MARROW TRAY 18G X 3

Recalls

DateFirmReason
2010-10-18Orthofix IncOuter cartons for the product may be labeled with incorrect needle gauge.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.