Home › INTEGRA MICROFRANCE › MicroFrance®
MicroFrance®
INTEGRA MICROFRANCE · Model 7779MF-5CC · UDI-DI 10381780089179
KCP
Prescription
4
510(k) clearances
26
Adverse events
1
Recalls
143
Facilities
Description
MicroFrance® ENT luer-lock 5 cc syringe
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-04-30 | Medegen Medical Products, LLC | Finished products were not sterilized. |
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.