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Sharn Inc

Sharn Anesthesia · Model S2020-P · UDI-DI 00817518022161

HOY
10
510(k) clearances
50
Adverse events
1
Recalls
719
Facilities

Description

EyeGard Pediatric

Recalls

DateFirmReason
2008-06-05Phillips Safety ProductsRadiation Protective Eyewear does not meet the radiation protection levels stated on the labeling.

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Data 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.