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INTEGRATION BROKER
Smith & Nephew, Inc. · Model 72201079 · UDI-DI 03596010589637
NFG
Prescription
0
510(k) clearances
39
Adverse events
1
Recalls
18
Facilities
Description
SOFTWARE INTEGRATION BROKER HL7
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-03-01 | Alcon Research, Ltd. | Alcon is conducting a voluntary medical device correction of all VERION Reference Units (Vision Planner) that are shared with the Alcon LenSx Laser System after receiving reports c |
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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.