Skip to content
Not a government website.Sources and limits

FDA recall 99679: Baxter Healthcare Corporation: Dextrose Injection

Build snapshot. Collected , once, when this site was built. It is not a live feed.

FDARecall 99679Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
Text from FDA, unedited.

FDA classification: Class I. FDA’s highest class: a reasonable probability that using the product will cause serious health consequences or death. Status: Ongoing.

Is it yours? Products and codes

  • Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06

    Lot or code
    Lot #: Y495066, Exp. Date July 31, 2027
    FDA recall number
    D-0850-2026
    Quantity
    606 bags

Distribution (FDA): U.S. Nationwide.

About this record

Issued by
U.S. Food and Drug Administration
Firm
Baxter Healthcare Corporation (other notices of this firm)
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99679 on September 16, 2026.

Other notices of Baxter Healthcare Corporation

Keep checking