cetrorelix acetatedrugHigh PriorityActive

Cetrorelix Acetate for Injection, 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90. Vial: Cetrorelix Acetate for Injection, 0.25 mg per vial, Mfd. for Meitheal Pharmaceuticals, Chicago, IL 6063

cetrorelix acetate Cetrorelix Acetate for Injection, 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90. Vial: Cetrorelix Acetate for Injection, 0.25 mg per vial, Mfd. for Meitheal Pharmaceuticals, Chicago, IL 6063 recalled by FDA. Defective Delivery System: Missing or duplicated needles within the injection kit

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source: FDA
Announced by source: February 9, 2026
Last reviewed by RecallRadar: March 4, 2026

What You Should Do

1## Cetrorelix Acetate for Injection, 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-
2Vial: Cetrorelix Acetate for Injection, 0.25 mg per vial, Mfd. for Meitheal Pharmaceuticals, Chicago, IL 6063 Agency: FDA | Category: drug Reason: Defective Delivery System: Missing or duplicated needles within the injection kit What to do:
3Stop using the product if your lot/model matches.
4Check the FDA notice for specifics.

Open Official Recall Notice Get Alerts for cetrorelix acetate Devices

What's Being Recalled

Quoted source excerpt from the official notice.

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

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot Q4E0112A, Exp.: 30 Apr 2027

#	Model
1	Lot Q4E0112A, Exp.: 30 Apr 2027

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my cetrorelix acetate device affected?

Check the affected models section on this page. The official notice currently lists Lot Q4E0112A, Exp.: 30 Apr 2027.

What is the remedy for this recall?

## Cetrorelix Acetate for Injection, 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90. Vial: Cetrorelix Acetate for Injection, 0.25 mg per vial, Mfd. for Meitheal Pharmaceuticals, Chicago, IL 6063 Agency: FDA | Category: drug Reason: Defective Delivery System: Missing or duplicated needles within the injection kit What to do: 1. Stop using the product if your lot/model matches. 2. Check the FDA notice for specifics. 3. Follow remedy instructions.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: cetrorelix acetate recall hub and Food & Drug recall hub.