FDA recall D-0024-2026

STAQ Pharma, Inc. · Class III · drug

Product

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

Distribution

Nationwide in the U.S.

Key facts

Status: Ongoing
Initiation date: 2025-10-09
Report date: 2025-10-22
Voluntary/Mandated: Voluntary: Firm initiated
Location: Denver, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0024-2026