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Anodyne Surgical
Psi/Eye-Ko, Inc. · Model AFK-0003 · UDI-DI 00840516142005
PZG
Prescription
0
510(k) clearances
4
Adverse events
6
Recalls
28
Facilities
Description
Anodyne Forsight Kit AFK-0003
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
| 2021-11-17 | Beaver Visitec International, Inc. | Kit packaging may have small holes compromising product sterility |
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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.