Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Menopur 75 IU Recalled by Ferring Pharmaceuticals Inc Due to Failed pH specifications: Out of Specification pH results...
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
Menopur 75 IU, (menotropins for injection), packaged as a) 5 single dose vials of Menotropins for injection, 5 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-2; b) Professional Sample Kit: 3 single dose vials of Menotropins for injection, 3 single dose vials of 0.9% Sodium Chloride Injection, USP 2 mL, NDC 55566-7501-3; Rx Only, Manufactured for Ferring Pharmaceuticals Inc. Parsippany. NJ 07054. Diluent manufactured for Ferring Pharmaceuticals Inc.
Quantity: 1,155,601 cartons/5 vials per carton 12546 physician samples
Why Was This Recalled?
Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chloride, USP
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