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CARDINAL HEALTH

Cardinal Health 200, LLC · Model 17-4561E · UDI-DI 10198956098077

OFZ Prescription
0
510(k) clearances
6
Adverse events
1
Recalls
17
Facilities

Description

BLOOD CULTURE TRAY

Recalls

DateFirmReason
2021-04-09Medical Action Industries, Inc. 306Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.

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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.