Why it was recalled
Presence of Particulate Matter; identified as stainless steel
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
Lot numbers, UPCs & expiration codes
Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
Where it was sold
USA Nationwide
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0743-2026
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- Jul 17, 2026
- FDA report date
- Aug 12, 2026
- Quantity
- 4,077 vials
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Sunny Pharmtech Inc.
Original FDA data
Every field from FDA enforcement report D-0743-2026, exactly as published.
Show all FDA fields
- City
- Taoyuan City
- Status
- Ongoing
- Country
- Taiwan
- Event ID
- 99437
- Address
- Hsinchu Science Park
- Address (line 2)
- No. 255 Longyuan 1st Rd.; Longtan Dist.
- Code information
- Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
- Report date
- Aug 12, 2026
- Product type
- Drugs
- Recall number
- D-0743-2026
- Classification
- Class I
- Recalling firm
- Sunny Pharmtech Inc.
- Product quantity
- 4,077 vials
- Reason for recall
- Presence of Particulate Matter; identified as stainless steel
- Voluntary / mandated
- Voluntary: Firm initiated
- 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
- Distribution pattern
- USA Nationwide
- Recall initiation date
- Jul 17, 2026
- Initial firm notification
- Letter
- Center classification date
- Aug 7, 2026