Sunny Pharmtech Cyclophosphamide Injection Recall: Stainless Steel Particulates
Sunny Pharmtech recalls Cyclophosphamide injection vials due to stainless steel particles that could cause serious injury. Affected vials were manufactured in Taiwan with specific lot numbers.
Stop using this now
Presence of Particulate Matter; identified as stainless steel
What happened, in plain English
Sunny Pharmtech is recalling Cyclophosphamide injection vials that may contain stainless steel particles. This could cause serious injury if the particles enter the bloodstream during injection. Read more at govinfonow.com/recall/309276-sunny-pharmtech-cyclophosphamide-injection-recall-stainless-steel-particulates.
Source Summary by GovInfoNow · govinfonow.com/recall/309276-sunny-pharmtech-cyclophosphamide-injection-recall-stainless-steel-particulates · Updated August 18, 2026 · FDA enforcement record: FDA #D-0744-2026
Cite this page
“Sunny Pharmtech Cyclophosphamide Injection Recall: Stainless Steel Particulates.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/309276-sunny-pharmtech-cyclophosphamide-injection-recall-stainless-steel-particulates. Based on FDA recall #D-0744-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0744-2026%22&limit=1).
Why it’s dangerous
Stainless steel particles can enter the bloodstream during injection, potentially causing serious injury or death. This risk occurs because the particles are not properly filtered from the injection solution.
Who’s affected
Prescription patients using Cyclophosphamide injections for cancer treatment. Those with the specific lot numbers and manufacturing details listed are most at risk.
How to tell if you have this one
Check for vials labeled 'Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only'. Look for lot number V24010V1 and expiration date 3/31/2027.
- Brand
Sunny Pharmtech- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Ongoing- Distribution
USA Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0743-2026 | 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 # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027 | 4,077 vials |
| D-0744-2026 | 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 # V24010V1, Exp 3/31/2027 | 1,464 vials |
What to do — step by step
Stop Using Now
Immediately discard the vial if it contains stainless steel particles that could cause serious injury.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “USA Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 26 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
Questions people ask
Where was this product manufactured?
Manufactured in Taiwan by Sunny Pharmtech for Long Grove Pharmaceuticals, LLC.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0744-2026 (July 17, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0744-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.