Ciprofloxacin Recall: Sandoz Otic Suspension Lot VNF35A
Announced 2026-06-24 · FDA
The FDA is recalling 1,680 bottles of Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension Rx Only, distributed to one consignee in California, due to temperature abuse. The affected lot is VNF35A with expiration date 08/31/2026. No corrective action information is provided in the recall notice.
| Brand | Sandoz Inc |
|---|---|
| Product | Ciprofloxacin 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 |
| Reason | Temperature Abuse |
| Severity | moderate |
| Units affected | 7803 |
| Distribution | Product was distributed to one consignee in CA. |
| Agency | FDA |
| Recall / campaign no. | Lot # VNF35A, Exp.08/31/2026 |
WHAT YOU SHOULD DO
- Do not use any bottle labeled with Lot VNF35A and expiration 08/31/2026.
- Contact the retailer or distributor to arrange recall return, replacement, or disposal of the recalled product.
- If you have used the product or have concerns, contact your healthcare provider for guidance.
- Visit the FDA recall notice or the distributor for additional instructions.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.