FDAFDA · Food and drugs·Recall number D-0237-2026
Cisatracurium Besylate Injection USP, 200mg/20mL*(10mg/mL), 10 x 20 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single dose 20mL vial NDC 70069-151-01; 10 x 20 Single dose vials per Carton, NDC 70069-151-10.
Published December 24, 2025 · Recall initiated: November 26, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Subpotent product:out of specification assay results observed during long term stability testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- CISATRACURIUM BESYLATE
- Manufacturer
- SOMERSET THERAPEUTICS LLC
- Distributor
- Nationwide in the USA
- UPC
- 0370069141014
- Lot
- Lot #: A250020, Exp Date 06/30/2026
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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