***URGENT DRUG RECALL NOTICE***
January 20, 2026
VIA EMAIL
Dear Valued Customer:
This is to inform you that one of our contract manufacturers, Wizcure Pharmaa Ltd., is recalling all lots of the following products that are within their expiration date. The Wizcure product has Omni Lens Private Ltd. on the label.
This is the only BioGlo product being recalled.
| Hilco Vision Item Number |
Product Description |
NDC# |
| 1030511 |
BioGlo (fluorescein sodium) Ophthalmic Strips, USP, 1mg - 100 |
17238-900-11 |
| 1030513 |
BioGlo (fluorescein sodium) Ophthalmic Strips, USP, 1mg - 300 |
17238-900-30 |
Wizcure Pharma is recalling the product because it was not manufactured in conformance with current good manufacturing practices.
This is a voluntary recall and applies only to products manufactured by Wizcure Pharmaa and is being conducted with the Food and Drug Administration's full knowledge and concurrence.
Immediately examine your inventory, quarantine any product subject to recall, and record the quantity of recalled inventory. The product is being recalled down to the RETAIL level. Attached is the list of specific lots sold by Hilco Vision.
You are required to return all product from the affected lots in your possession. To implement this recall, please complete the attached verification form and follow these instructions:
- Check your Stock and Verify Packaging: Look for the Omni Lens Private Ltd. label and NDC numbers associated with these products to determine if you have any product from the affected lots.
- If so, immediately discontinue use of the affected lots.
- URGENT – The attached “Urgent Drug Recall Response Form” must be completed and returned to us by March 3, 2026. Please complete and return the attached form even if you do not have the recalled product.
- Once we receive your Product Recall Form, we will issue you a return label to send the product back to us (if you have affected inventory). Your credit will be issued after we receive the returned product. Please allow time to receive both your return label and your credit. Once received, use your return label to ship the recalled product. Do not return your recalled product prior to receiving the RMA. To receive credit, all product must be returned.
If you should have any questions, please call (800) 955-6544.
We apologize for the inconvenience. Thank you for your cooperation and support.
Sincerely,
David C. Hufnagle, Ph.D.
Vice President of Global QARA