Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring Pharmaceuticals Inc Due to Labeling; incorrect or missing insert; Warnings portion of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ferring Pharmaceuticals Inc directly.
Affected Products
Novarel¿ (Chorionic Gonadotropin for injection, USP), 10,000 USP FOR INTRAMUSCULAR USE ONLY Rx Only NDC 55566-1501-0 Manufactured for : Ferring Pharmaceuticals Inc., Parsippany, NJ 07054 Manufactured by: DRAXIS Specialty Pharmaceuticals Inc., Quebec, Canada. NDC # 55566-1501-0 is assigned to the vial of NOVAREL and is displayed on the vial label. NDC # 55566-1501-1 is assigned to the unit of sale, which is a carton containing 1 vial of NOVAREL and 1 vial of diluent along with the insert. NDC # 55566-1501-1 is displayed on the unit of sale and is the item subject to recall.
Quantity: 146,867 Vials
Why Was This Recalled?
Labeling; incorrect or missing insert; Warnings portion of the Package Insert is missing the warning statement: Anaphylaxis has been reported with urinary-derived hCG products.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ferring Pharmaceuticals Inc
Ferring Pharmaceuticals Inc has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report