Aurolab Trust recall: FOCUS PI Hypromellose 0.7% Formula
Aurolab Trust is recalling FOCUS PI Hypromellose 0.7% Formula because of a sterility problem – 25,220 bottles. The U.S. Food and Drug Administration published the recall on October 7, 2026; it began on September 17, 2026. Distributed in 1 state (Virginia).
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | FOCUS PI Hypromellose 0.7% Formula |
| Brand | Aurolab Trust |
| Type | Drugs |
| Classification | Class II |
| Recall date | September 17, 2026 |
| Published by FDA | October 7, 2026 |
| Quantity | 25,220 bottles |
| Recall ID | 99903 |
Recalled products
- FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109. NDC: 82724-007-19
- FDA recall number
- D-0874-2026
- Codes, lots and dates
- Batch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28
- Quantity
- 25,220 bottles
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99903
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Madurai, India
Why it was recalled
The problem: a sterility problem.
The reason the FDA lists: “Lack of Assurance of Sterility”
Where it was sold
1 state: Virginia. Distribution as the FDA records it: “VA”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99903, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is Aurolab Trust FOCUS PI Hypromellose 0.7% Formula recalled?
Yes. Aurolab Trust recalled it on September 17, 2026; FDA published it October 7, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of a sterility problem. The reason given: Lack of Assurance of Sterility
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
In 1 state (Virginia).
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.