Class III · Lower riskActive recall
Ketamine Hydrochloride
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberLot #: 25156673A, Expiry: 02FEB2026.
Where it was soldNationwide in the U.S.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Labeling: Incorrect or Missing Lot and/or Exp Date
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | STAQ Pharma, Inc. |
| NDC | 73177-0156-02 |
Show the full FDA record
| Full product label | 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. |
| Recalling firm | STAQ Pharma, Inc. |
| Distribution | Nationwide in the U.S. |
| Recall initiated | 2025-10-09 |
| Report date | 2025-10-22 |
| Recall completed | — |
| Recall number | D-0024-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Denver CO United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.