Drug recall D-0569-2023
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
Reason for recall
Presence of Particulate Matter: A piece of glass was found in a prefilled syringe.
Lots and codes
Lot #: HAD1190A, Exp. 02/2024
Recall details
- Recalling firm
- Sun Pharmaceutical Industries Ltd., Halol, N/A
- Quantity
- 24194 Prefilled Syringes
- Distribution
- Nationwide in the USA
- Type
- N/A
- Recall initiated
- April 19, 2023
- Terminated
- December 13, 2023
Related products
- Fyremadel – drug information
- NDC 55566-1010 Fyremadel · Ganirelix Acetate 250 ug/.5mL · Ferring Pharmaceuticals Inc.