Home › C. R. Bard, Inc. › Bard® CritiCore® Collection Container
Bard® CritiCore® Collection Container
C. R. Bard, Inc. · Model 153200 · UDI-DI 00801741019357
FFG
Prescription
10
510(k) clearances
557
Adverse events
1
Recalls
37
Facilities
Description
Bard® CritiCore® Collection Container
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-04 | Cardinal Health 200, LLC | Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.