Class II

Drug Recall: Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.

Meitheal Pharmaceuticals, Inc · February 9, 2026

Reason for Recall

Defective Delivery System: Missing or duplicated needles within the injection kit

Distribution

U.S. Nationwide

States Affected

NATIONWIDE

Quantity Affected

16,477 kits

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0340-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.