FDA Import Refusal 1FX-4289807-3/10001/1 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1317628

The FDA refused shipment 1FX-4289807-3/10001/1 from Bausch & Lomb Incorporated (United States) on Sep 18, 2026. The refused product falls under Devices — DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Sep 18, 2026
Country
United States
Product Category
Devices
Product Code
86QIT DAILY WEAR SOFT CONTACT LENS TO REDUCE THE PROGRESSION OF MYOPIA
Charges
118