Cyclophosphamide for Injection (D-0743-2026) Recall: Particulate Matter
Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL…
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Cyclophosphamide for Injection recalled?
Presence of Particulate Matter; identified as stainless steel
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
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
Which lot codes, UPCs or models are affected?
Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
- Agency record number
- D-0743-2026
- Product
- Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL…
- Recalling firm
- Sunny Pharmtech Inc.
- Quantity
- 4,077 vials
- Distribution
- USA Nationwide
- Recall started
- July 17, 2026
- Report date
- August 12, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)