# FDA recall D-0340-2026

> **Meitheal Pharmaceuticals, Inc** · Class II · drug recall initiated 2026-02-09.

## 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

- **Recall number:** D-0340-2026
- **Recalling firm:** Meitheal Pharmaceuticals, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-02-09
- **Report date:** 2026-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

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

## Citation

> AI Analytics. FDA recall D-0340-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0340-2026. Source: US FDA. Licensed CC0.

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