Ferring Pharmaceuticals Inc

Complete recall history across all FDA and CPSC categories — 12 total recalls

Ferring Pharmaceuticals Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (12)

FDA drug safety enforcement actions by Ferring Pharmaceuticals Inc

Date Product Reason Class
Jun 12, 2023 Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 va... cGMP deviations: potential for Microbial Contamination of Non-Sterile Products Class II
Mar 11, 2021 ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACT... Defective Delivery System: customer complaints concerning the injector pen br... Class II
Mar 11, 2021 ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMAC... Defective Delivery System: customer complaints concerning the injector pen br... Class II
Mar 2, 2021 Menopur 75 IU, (menotropins for injection), packaged as a) 5 single dose vial... Failed pH specifications: Out of Specification pH results for 0.9% Sodium Chl... Class III
Jul 21, 2020 DDAVP Nasal Spray (desmopressin acetate) 10 mcg/0.1 mL, 5 mL bottles, Rx Only... Superpotent Drug Class I
Jul 21, 2020 Desmopressin Acetate Nasal Spray 10 mcg/0.1 mL, 5mL glass vial with spray cap... Superpotent Drug Class I
Jul 21, 2020 STIMATE (desmopressin acetate) Nasal Spray1.5 mg/mL, 2.5 mL glass vial with s... Superpotent Drug Class I
Sep 9, 2015 Bravelle 75 IU (urofollitropin for injection, purified) For Subcutaneous or I... Subpotent Drug Class III
Apr 28, 2014 TEV-TROPIN [somatropin (rDNA origin) for injection] 5 mg (15 IU) 1-count bott... Chemical Contamination: TEV-TROPIN [somatropin (rDNA origin) for injection] m... Class II
Sep 19, 2013 ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP, 21 inserts, Rx Only, Man... Discoloration; due to prolonged heat exposure. Class III
Feb 1, 2013 TEV-TROPIN (somatropin (rDNA origin) for injection) 5 mg (15 IU). Prescripti... Labeling: Label Mix-up: Units of Lot 201131320087 are packaged in cartons lab... Class III
Aug 23, 2012 Novarel¿ (Chorionic Gonadotropin for injection, USP), 10,000 USP FOR INTRAMUS... Labeling; incorrect or missing insert; Warnings portion of the Package Insert... Class III

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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