Nubratori recalls Dexonto 0.4% solution 20mg/5mL vials due to incorrect expiration dates on some boxes. The outer box shows a BUD of 12/25/2025 instead of the correct 12/25/2024. This may lead to expired medication use.
Labeling: Incorrect or Missing Lot and/or Expiration date: Individual vials of Dexonto 0.4%, are labeled correctly with the BUD of 12/25/2024, however, the outer box on some of the Dexonto 0.4% are labeled incorrectly with a BUD of 12/25/2025.
Nubratori is recalling Dexonto 0.4% (dexamethasone sodium phosphate) solution vials because some boxes have incorrect expiration dates. Using these vials could lead to expired medication that might not be safe for medical use.
The outer box of some vials shows an expiration date of December 25, 2025 instead of the correct December 25, 2024. This could mean the medication expires later than intended, potentially leading to expired medication that might not be safe for medical use.
Prescription users of Dexonto 0.4% solution for iontophoresis who received the recalled vials with incorrect expiration dates on the outer box. Patients using this medication for medical purposes are most at risk.
Check for the outer box labeled with a BUD of 12/25/2025 instead of 12/25/2024. The product is sold as 12-5 mL single dose units per box with NDC 71300-6564-1 (box) and 71300-6564-3 (vial).
Verify the expiration date on the outer box. If it shows 12/25/2025 instead of 12/25/2024, this vial is part of the recall.
Nubratori is recalling Dexonto 0.4% solution vials because some outer boxes have incorrect expiration dates (showing 12/25/2025 instead of 12/25/2024).
Check the expiration date on the outer box. If it shows 12/25/2025 instead of 12/25/2024, stop using it and contact Nubratori for instructions.
The recall record does not specify a remedy. You should check the expiration date and contact Nubratori if you have the recalled product.
We’ve drafted a message you can send Nubratori to request your refund or repair — edit it as you like.
Subject: Recall D-0392-2025 — Nubratori Nubratori Hello, I own a Nubratori that is covered by recall D-0392-2025 from Nubratori. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
