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Visitec®
Beaver-Visitec International, Inc. · Model 8590300 · UDI-DI 30886158010129
HOY
Prescription
10
510(k) clearances
51
Adverse events
1
Recalls
720
Facilities
Description
EYE BANDAGE GUIBOR BUBBLE BANDAGE STERILE 10/BX
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-06-05 | Phillips Safety Products | Radiation Protective Eyewear does not meet the radiation protection levels stated on the labeling. |
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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.
