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Class II · ModerateActive recall

Focus Pi

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberBatch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28
Where it was soldVA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Lack of Assurance of Sterility

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byCOVALENT MEDICAL
Brand nameFOCUS PI
Generic nameHYPROMELLOSE EYE DROPS 0.7%
Active ingredient(s)HYPROMELLOSE 2910 (4000 MPA.S)
Distributed by / forCovalent Management, Inc., Manassas, VA 20109
NDC82724-007-19
Show the full FDA record
Full product labelFOCUS 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
Recalling firmAurolab Trust
DistributionVA
Quantity25,220 bottles
Recall initiated2026-09-17
Report date2026-10-07
Recall completed—
Recall numberD-0874-2026
ClassificationClass II
FDA statusOngoing
Origin on fileMadurai India

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.