FDAFDA · Food and drugs·Recall number D-1379-2020
Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD 02370, NDC: 44087-1225-1
Published July 15, 2020 · Recall initiated: June 29, 2020
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
Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- CETROTIDE
- Manufacturer
- EMD Serono, Inc.
- Distributor
- Nationwide in the US
- Lot
- Lot # 8J025A; 8J025B, Exp 09/30/2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.