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 |
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.
How to identify the recalled item
| Lot / date codes | Lot # VNF35A, Exp.08/31/2026 |
|---|---|
| Lot / date codes | Lot VA0099422; Exp. Date June 30, 2028 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
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.