STAQ Pharma, Inc. 2025-10-22 Health moderate FDA
Health · FDA · Recall #FDA-D-0024-2026
Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ… Recall
Issued October 22, 2025 · STAQ Pharma, Inc.
In October 2025, STAQ Pharma, Inc. recalled the Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ…, a moderate health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Labeling: Incorrect or Missing Lot and/or Exp Date
What you should do
- 1 Stop using Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact STAQ Pharma, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- STAQ Pharma, Inc.
- Category
- Health
- Recall date
- October 22, 2025
- Units affected
- Not reported
- Sold at
- Nationwide in the U.S.
- Recall number
- FDA-D-0024-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- STAQ Pharma, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.