Ketamine Hydrochloride recall: Labeling Error
Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC…
Why was Ketamine Hydrochloride recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 25156673A, Expiry: 02FEB2026.
- 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…
- Recalling firm
- STAQ Pharma, Inc.
- Distribution
- Nationwide in the U.S.
- Recall date
- October 22, 2025
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)