Home › Cardinal Health, Inc. › Argyle
Argyle
Cardinal Health, Inc. · Model 8881443009 · UDI-DI 10884521158207
10
510(k) clearances
9
Adverse events
1
Recalls
142
Facilities
Description
Oral Evacuator,Opaque
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-02 | Stradis Medical, LLC dba Stradis Healthcare | Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in |
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.