Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc...
FDA Recall #D-0024-2026 — Class III — October 9, 2025
Product Description
Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02.
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Recalling Firm
STAQ Pharma, Inc. — Denver, CO
Classification
Class III — Not likely to cause adverse health consequences.
Product Type
Drugs
Distribution
Nationwide in the U.S.
Code Information
Lot #: 25156673A, Expiry: 02FEB2026.
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated