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Class II · ModerateActive recall

Ciprofloxacin And Dexamethasone

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

Does this affect you?
Check your lot numberLot # VNF35A, Exp.08/31/2026
Where it was soldProduct was distributed to one consignee in CA.
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

Temperature Abuse

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 byNovartis Manufacturing NV, Belgium, Distributed by: Sandoz, Inc., Princeton, NJ
Brand nameCIPROFLOXACIN AND DEXAMETHASONE
Generic nameCIPROFLOXACIN AND DEXAMETHASONE
Active ingredient(s)CIPROFLOXACIN HYDROCHLORIDE, DEXAMETHASONE
Distributed by / forSandoz, Inc., Princeton, NJ
NDC0781-6186-67
Show the full FDA record
Full product labelCiprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension Rx Only, For Use in Ears Only, Manufactured By: Novartis Manufacturing NV, Belgium, Distributed by: Sandoz, Inc., Princeton, NJ, NDC# 0781-6186-67, Carton NDC# 0781-6186-67
Recalling firmSandoz Inc
DistributionProduct was distributed to one consignee in CA.
Quantity1,680 bottles
Recall initiated2025-08-13
Report date2025-09-17
Recall completed—
Recall numberD-0626-2025
ClassificationClass II
FDA statusOngoing
Origin on filePrinceton NJ United States

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.