Home › Alcon Laboratories, Inc. › ISPAN
ISPAN
Alcon Laboratories, Inc. · Model 8065797105 · UDI-DI 00380657971053
LPO
Prescription
0
510(k) clearances
504
Adverse events
1
Recalls
3
Facilities
Description
ISPAN C3F8 CONSTELLATION 125GM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-11-18 | Alcon Laboratories, Inc | The firm initiated the recall on 11/18/2003 via letters to all consignees. The letter advises physicians to stop using any patient bracelets (blue color) that contain the word 'st |
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.