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Class IOngoing

Sunny Pharmtech Inc. recalls 2 products

Recall date · record updated Aug 12, 2026 · Source: U.S. Food and Drug Administration (openFDA drug enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Sunny Pharmtech Inc.
Reason
Presence of Particulate Matter; identified as stainless steel
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
USA Nationwide
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99437…

Products (2)

  1. 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

    Codes/lots: Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027Quantity: 4,077 vialsRecall no. D-0743-2026Class I

  2. 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

    Codes/lots: Lot # V24010V1, Exp 3/31/2027Quantity: 1,464 vialsRecall no. D-0744-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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