WhichRecall
Class IIReported 2025-05-07

Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL), Rx Only, 12 - 5 mL Single Dose Units per box, Preservative Free, For Iontophoresis Use Only, Non-Sterile Product, Not for Injection, NUBRATORI RX, 381 Van Ness Ave# 1507, CA 90501, NDC 71300-6564-1 (box), 71300-6564-3 (vial).

Recalled by Nubratori, Inc

Reason for Recall

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.

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Recall Number
D-0392-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-04-15
Reported
2025-05-07
Distribution
PA and CA.
Code Info
Lot #: C04292401X1, BUD: 12/25/2025 (box).
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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