Class III

Drug Recall: 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.

STAQ Pharma, Inc. · October 9, 2025

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date

Distribution

Nationwide in the U.S.

States Affected

NATIONWIDE

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0024-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.