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Bone Marrow Collection/Transfusion Kit
FDA product code LWE · Class 2 · Unknown
68
Registered devices
46
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
N/A — CAREFUSION 2200, INCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.SpineSmith Fusionary Graft Delivery System — Celling BiosciencesCARDINAL HEALTH — Cardinal Health 200, LLCMedical Action Industries — MEDICAL ACTION INDUSTRIES INC.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCAero-Med — AERO-MED, LLCSpineSmith Fusionary Graft Delivery System — Celling BiosciencesCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCJamshidi — CAREFUSION 2200, INCSpineSmith Fusionary Graft Delivery System — Celling BiosciencesCARDINAL HEALTH — Cardinal Health 200, LLCBone Marrow Collection Kit with Flexible Pre-Filter and Inline Filters — Fresenius Kabi AGCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCJamshidi — CAREFUSION 2200, INCSpineSmith Fusionary Graft Delivery System — Celling BiosciencesBilateral BMA Kit — Biomet Biologics, LLCBone Marrow Collection Kit with Flexible Pre-Filter and Inline Filters — Fresenius Kabi AG
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-10-18 | Orthofix Inc | Outer cartons for the product may be labeled with incorrect needle gauge. |
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