FDAFDA recall D-0744-2026 · Aug 12, 2026
Sunny Pharmtech Inc.: Cyclophosphamide for Injection recall
Recall found
Product
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
Reason for recall
Presence of Particulate Matter; identified as stainless steel
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Lot # V24010V1, Exp 3/31/2027
- Quantity
- 1,464 vials
- Distribution
- USA Nationwide
- Recalling firm
- Sunny Pharmtech Inc., Taoyuan City
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-17
Source: openFDA enforcement record D-0744-2026 · search recall number D-0744-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.