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CARDINAL HEALTH
Cardinal Health 200, LLC · Model 07-4432B · UDI-DI 10198956207639
OFM
Prescription
0
510(k) clearances
0
Adverse events
2
Recalls
17
Facilities
Description
CENTRAL LINE BLOOD DRAW KIT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-04-09 | Medical Action Industries, Inc. 306 | Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. |
| 2010-12-06 | Continental Medical Labs,Inc | Continental Medical labs, Inc, is recalling various lots of Blood Center Kit and Port VAD Kits because Covidien reported that testing could not pick up an Over-Sulfated Chondro |
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Get your free API keyRead the docsData 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.