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FDA recall 99437: Sunny Pharmtech Inc.: Cyclophosphamide for Injection and 1 more

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FDARecall 99437Medicines

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; identified as stainless steel
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

  • Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

    Lot or code
    Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
    FDA recall number
    D-0743-2026
    Quantity
    4,077 vials
  • Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1

    Lot or code
    Lot # V24010V1, Exp 3/31/2027
    FDA recall number
    D-0744-2026
    Quantity
    1,464 vials

Distribution (FDA): USA Nationwide

About this record

Issued by
U.S. Food and Drug Administration
Firm
Sunny Pharmtech Inc.
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; identified as stainless steel”

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 99437 on August 12, 2026.

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