The Recall Desk
HighFDA (Drugs)·D-0435-2026·Announced 2026-04-15

[pending] DEXTROSE (DEXTROSE MONOHYDRATE)

Pending LLM rewrite. Source: FDA_DRUG D-0435-2026.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

Lack of Assurance of Sterility

The recalled product

Product
DEXTROSE (DEXTROSE MONOHYDRATE)
Brand
DEXTROSE
Manufacturer
Fresenius Kabi USA, LLC

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Batch# 6402296
  • Exp Date: 07/31/2026.

Distribution

Distributed nationwide across the United States.

Same brand · DEXTROSE