FDAFDA · Food and drugs·Recall number D-0569-2023
Fyremadel (ganirelix acetate) injection, 250 mcg/0.5 mL, One Single Dose Sterile Prefilled Syringe 0.5 mL, For Subcutaneous Use, Rx Only, Sterile, Distributor: Ferring Pharmaceuticals Inc., Parsippany, NJ 07054, USA, NDC 55566-1010-1
Published May 3, 2023 · Recall initiated: April 19, 2023
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Recall details
- Brand
- FYREMADEL
- Manufacturer
- Sun Pharmaceutical Industries Ltd.
- Distributor
- Nationwide in the USA
- Lot
- Lot #: HAD1190A, Exp. 02/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- India
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