Fresh Recalls

FDAClass I · Drug · Recall D-0743-2026 · Recalled August 12, 2026

Cyclophosphamide for Injection recall — Sunny Pharmtech Inc.

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Cyclophosphamide for Injection
Company / brand
Sunny Pharmtech
Lot / serial / date codes
Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
Distribution
USA Nationwide
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Presence of Particulate Matter; identified as stainless steel

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Cyclophosphamide for Injection

3. Open the official notice or contact

Official recall ID
D-0743-2026
Brand
Sunny Pharmtech
Classification
Class I
Units affected
4,077 vials
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Taoyuan City, Taiwan
Firm address
Hsinchu Science Park, No. 255 Longyuan 1st Rd.; Longtan Dist., N/A

Identifying details (verbatim from the notice)

Product codes / lots
Lot # C23019V1, Exp 10/31/2026; C24015V1, Exp 4/30/2027
Distribution
USA Nationwide
Firm notified the public via
Letter
FDA event ID
99437
Recall initiated
July 17, 2026
FDA classified
August 7, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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