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Bone Marrow Collection Stand

Fresenius Kabi AG · Model X6R2105 · UDI-DI 04086000100380

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

Description

For use with Bone Marrow Collection Kit

Recalls

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

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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.