Quick Facts at a Glance
- Recall Date
- May 12, 2026
- Hazard Level
- HIGH
- Brands
- DOXORUBICIN HYDROCHLORIDE, NorthStar RxLLC
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- DOXORUBICIN HYDROCHLORIDE, NorthStar RxLLC
- Model numbers
- Lot HAG2581B, expires: 05/31/2027
- UPC codes
- 72603-103, 72603-200, 72603-103-01, 72603-200-01
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 12, 2026
Reported by FDA DRUG
June 17, 2026
RecallRadar source check
June 23, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Presence of Particulate matter: Particulate matter identified as glass.
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact SUN PHARMACEUTICAL INDUSTRIES INC or your healthcare provider for guidance. Notification method: E-Mail
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Full Description
DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-dose vials, Sterile, Rx only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol, Gujarat, India, NDC 72603-200-01.. Generic: DOXORUBICIN HYDROCHLORIDE; Brand: DOXORUBICIN HYDROCHLORIDE. Reason: Presence of Particulate matter: Particulate matter identified as glass.. Classification: Class I. Quantity: 675 vials. Distribution: U.S. Nationwide
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Safety Guide
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