Sun Pharmaceutical recalls Fyremadel (ganirelix acetate) injections with a glass particle found in some prefilled syringes. This could cause injury if injected. Stop using and contact your doctor.
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Sun Pharmaceutical is recalling Fyremadel injections that contain a glass particle. This could cause injury if injected, so affected users should stop using the product and contact their doctor.
A glass particle was found in some prefilled syringes. If injected, this could cause injury such as a cut or infection. The product is for subcutaneous use only.
People who have received a Fyremadel injection with a glass particle in the syringe. Those using the product for fertility treatment are most at risk.
Check the product label for the lot number HAD1190A and expiration date 02/2024. The product is a 250 mcg/0.5 mL injection for subcutaneous use only.
Immediately stop using the Fyremadel injection if you have the recalled product.
No, the product contains a glass particle that could cause injury if injected.
Check the product label for lot number HAD1190A and expiration date 02/2024.
Stop using the product and contact your doctor immediately.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0569-2023 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0569-2023 from Sun Pharmaceutical. 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.
