Click here: to donate by Credit Card
Or here: to donate by PayPal
Or by mail to: Free Republic, LLC - PO Box 9771 - Fresno, CA 93794
Thank you very much and God bless you.
Posted on 07/10/2026 8:22:32 AM PDT by V_TWIN
The Food and Drug Administration announced the recall of millions of bottles of eye drops because they may contain a foreign substance.
The agency classified the recall as a Class II, meaning it is "a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
The eye drops are used “to treat non-infectious eye allergies and inflammation, including damage caused by chemical and thermal burns,” the Mayo Clinic said.
The prescription eye drops came in three sizes: 5 mL (NDC 70748-332-02), 10 mL (NDC 70748-332-03) and 15 mL (NDC 70748-332-04).
|
|
Click here: to donate by Credit Card Or here: to donate by PayPal Or by mail to: Free Republic, LLC - PO Box 9771 - Fresno, CA 93794 Thank you very much and God bless you. |
Recalled medicine ping!
Tainted eyedrops — usually from overseas manufacturers— are a recurring problem. My sister lost sight in one eye after a single use of OTC eyedrops imported from India.
Both recalls are from India................Hmmmm, I wonder if there’s a connection?............🤔
Product Details
Product Description:
prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC 70748-332-02); b) 10 mL (NDC 70748-332-03), c) 15 mL (70748-332-04), Manufactured by: Lupin Limited, Pithampur (M.P) 454 775, INDIA
Reason for Recall:
Presence of Foreign Substance
Product Quantity:
2,530,182 bottles
Recall Number:
D-0655-2026
Code Information:
Lots: a) HA00937, HA00939, HA00941, HA00971, H00973, HA00975, Expires: 7/31/2026; HA00987, HA00989, HA00991, HA01010, HA01012, HA01014, HA01016, HA01048, Expires: 8/31/2026; HA01120, HA01137, HA01129, HA01138, HA01133, Expires: 9/30/2026; HA01148, HA01196, HA01198, HA01200, HA01206, HA01208, HA01210, HA01212, HA01214, HA01216, HA01218, HA01220, Expires: 10/31/2026; HA01236, HA01238, HA01240, HA01244, HA01246, HA01248, HA01261, HA01263, HA01265, more...
Classification:
Class II
Event Details
Event ID:
99144
Voluntary / Mandated:
Voluntary: Firm initiated
Product Type:
Drugs
Initial Firm Notification of Consignee or Public:
Letter
Status:
Ongoing
Distribution Pattern:
U.S. Nationwide
Recalling Firm:
Lupin Pharmaceuticals Inc.
5801 Pelican Bay Blvd Ste 500
Naples, FL 34108-2734
United States
Press Release URL(s):
Press Release Not Issued For This Recall
Recall Initiation Date:
6/4/2026
Center Classification Date:
6/30/2026
Date Terminated:
N/A
The connection is Indians should stay in their IT swim lane and stay the heck out if the pharmaceutical industry!
The parts of Indi I have been to were FILTHY DIRTY! One bathroom for one apartment BUILDING!
Very strange that they haven’t reported the analysis of what the “foreign substance” is. Was it visible to naked eye? Was it a specific color? Chemical? Biological?
I would guess that some kind of analysis had to be done.
Bookmark
cant imagine the chaos during diarrhea outbreaks
Disclaimer: Opinions posted on Free Republic are those of the individual posters and do not necessarily represent the opinion of Free Republic or its management. All materials posted herein are protected by copyright law and the exemption for fair use of copyrighted works.