OVERLOOKED

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Class IIOngoing

Aurolab Trust recalls FOCUS PI Hypromellose 0

Recall date · record updated Oct 7, 2026 · Source: U.S. Food and Drug Administration (openFDA drug enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Aurolab Trust
Reason
Lack of Assurance of Sterility
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
VA
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99903…

Products

  1. 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

    Codes/lots: Batch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28Quantity: 25,220 bottlesRecall no. D-0874-2026Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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