Lupin Pharmaceuticals recalls Ganirelix Acetate injection due to impurities in the product. This may affect patients using the medication. Contact the manufacturer for details.
Failed impurities/degradation specifications: out of specification results for Ganirelix acetate acrylic acid adduct impurity.
Lupin Pharmaceuticals is recalling Ganirelix Acetate injections because they contain impurities that could be harmful. This recall affects patients who have been prescribed this medication for fertility treatments.
The product contains impurities that may not be safe for medical use. These impurities could cause harm to patients receiving the injection. The specific risk is not clearly described in the recall notice.
Patients prescribed Ganirelix Acetate injections for fertility treatments are affected. Those using the recalled product may be at risk due to potential impurities.
Check for the product name 'Ganirelix Acetate Injection, 250 mcg/0.5mL, Single-dose Sterile Prefilled Syringe, 27 gauge by 1/2' needle' on the label. The product was manufactured by Lupin Pharmaceuticals and sold with NDC 70748-274-01.
Look for the product name and NDC number 70748-274-01 on the label.
The recall states the product has impurities that may not be safe, but the specific risk is not clearly described.
The recall does not provide a remedy, so contact Lupin Pharmaceuticals for further instructions.
Check the product label for the name 'Ganirelix Acetate Injection, 250 mcg/0.5mL, Single-dose Sterile Prefilled Syringe, 27 gauge by 1/2' needle' and NDC 70748-274-01.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0220-2026 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0220-2026 from Lupin Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
