Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Glycopyrrolate Injection Recalled by Meitheal Pharmaceuticals Inc Due to Failed Impurities/Degradation Specifications
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Meitheal Pharmaceuticals Inc directly.
Affected Products
Glycopyrrolate Injection, USP 4mg per 20mL, 20 mL Multi-Dose Vials, Rx only, Mfd for Meitheal Pharmaceuticals, Chicago, IL 60631. NDC 71288-408-21
Quantity: 1,160 ten-pack cartons
Why Was This Recalled?
Failed Impurities/Degradation Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Meitheal Pharmaceuticals Inc
Meitheal Pharmaceuticals Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report