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Evert-It
Mai/Genesis · Model 36000 · UDI-DI 00683693360004
1
510(k) clearances
82
Adverse events
2
Recalls
92
Facilities
Description
Evert-It Nipple Enhancer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-12 | Ameda, Inc. | Devices were not sterilized |
| 2015-02-12 | Ameda, Inc. | Devices were not sterilized |
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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.