Sun Pharmaceutical Industries Ltd. recalls Fyremadel (ganirelix acetate) injection, 250 mcg/0.5 mL, One Single Dose Sterile Prefilled Syringe 0.5 mL, For Subcutane
Recalled May 3, 2023 · FDA recall D-0569-2023 · Sun Pharmaceutical Industries
Hazard
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe. · FDA Class II
Units
24194 Prefilled Syringes
Sold at
Nationwide in the USA
Description
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Product
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
Manufacturer(s)
Sun Pharmaceutical Industries Ltd.
Made in
India
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →