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Bone Marrow Collection/Transfusion Kit

FDA product code LWE · Class 2 · Unknown

69
Registered devices
46
Adverse events
1
Recalls
3
510(k) clearances

Devices with this code

CARDINAL HEALTH — Cardinal Health 200, LLCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.CARDINAL HEALTH — Cardinal Health 200, LLCN/A — CAREFUSION 2200, INCJamshidi — CAREFUSION 2200, INCJamshidi — CAREFUSION 2200, INCJamshidi — CAREFUSION 2200, INCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCBioAccess Marrow Collection System — BIOACCESS INCAero-Med — AERO-MED, LLCCARDINAL HEALTH — Cardinal Health 200, LLCBone Marrow Collection Kit with Flexible Pre-Filter and Inline Filters — Fresenius Kabi AGSpineSmith Fusionary Graft Delivery System — Celling BiosciencesN/A — CAREFUSION 2200, INCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCJamshidi — CAREFUSION 2200, INC

Recent recalls

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

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.