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Bausch + Lomb
Bausch & Lomb Incorporated · Model E0421 · UDI-DI 00757770409761
HMZ
Prescription
0
510(k) clearances
28
Adverse events
1
Recalls
34
Facilities
Description
TRAB HARMS W/HDL PAIR 1RT-1LT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-09-06 | Iantrek Inc. | Potential for compromised integrity of the sterile packaging. |
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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.