STAQ Pharma recalls 50mL single-dose hydro morphine syringes with incorrect morphine sulfate labeling. This could lead to medication errors if used without proper identification.
Labeling: Label Mix up; A limited number of syringes containing HYDROmorphone HCl PF were incorrectly labeled as Morphine Sulfate PF with lot number 21104221A
STAQ Pharma is recalling a limited number of hydro morphine syringes that were incorrectly labeled as morphine sulfate. This could cause serious medication errors if someone uses the wrong drug.
The syringes were incorrectly labeled as morphine sulfate instead of hydro morphine. This could lead to medication errors if someone uses the wrong drug without proper identification.
People who have the specific lot number 21104221A syringes with hydro morphine labeling. Healthcare providers and patients using prescription-only hydro morphine syringes are most at risk.
Check for lot number 21104221A on the syringe label. The product is a 50mL single-dose hydro morphine syringe with NDC 73177-0104-05.
Verify the label shows hydro morphine HCl PF, not morphine sulfate PF.
The product is safe to use only if the label correctly identifies it as hydro morphine HCl PF. Incorrect labeling could lead to medication errors.
Check the label for lot number 21104221A. If it matches, contact STAQ Pharma for guidance.
Look for lot number 21104221A on the syringe label. The product is a 50mL single-dose hydro morphine syringe with NDC 73177-0104-05.
We’ve drafted a message you can send STAQ Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0633-2022 — STAQ Pharma STAQ Pharma Hello, I own a STAQ Pharma that is covered by recall D-0633-2022 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.
