STAQ Pharma recalls 50mL ketamine IV injection with missing lot or expiration date. Patients should check labels for correct dates to avoid medication errors.
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma is recalling a specific ketamine injection product due to missing or incorrect lot and expiration dates on the label. This could lead to medication errors if the wrong batch is used.
The injection comes with a label that may not show the correct lot number or expiration date. This could cause medication errors if healthcare providers use the product without checking the label.
Healthcare professionals using this ketamine injection for IV procedures in the U.S. are most at risk if they use the product without verifying the label dates.
Check the label for lot number 25156673A and expiration date February 2026. This product was sold by STAQ Pharma in the U.S. with NDC 73177-0156-02.
Verify the lot number and expiration date on the product label. If missing or incorrect, do not use the product.
The recall is for missing or incorrect lot and expiration dates, not the product itself. If the label is correct, the product is safe.
Look for the lot number 25156673A and expiration date February 2026 on the label. This product was sold by STAQ Pharma with NDC 73177-0156-02.
Check the label for the correct lot number and expiration date. If missing or incorrect, do not use the product.
We’ve drafted a message you can send STAQ Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0024-2026 — STAQ Pharma STAQ Pharma Hello, I own a STAQ Pharma that is covered by recall D-0024-2026 from STAQ Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
