FDA recall D-0340-2026

Meitheal Pharmaceuticals, Inc · Class II · drug

Product

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.

Reason for recall

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

Distribution

U.S. Nationwide

Key facts

Status
Ongoing
Initiation date
2026-02-09
Report date
2026-02-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Chicago, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0340-2026