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AESCULAP
AESCULAP, INC. · Model MA011R · UDI-DI 04046964580420
KCB
Prescription
1
510(k) clearances
8
Adverse events
1
Recalls
109
Facilities
Description
KILLIAN Suction Cannula, 5", (125 mm), small, #1, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
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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.