STAQ Pharma Morphine Sulfate Syringes Recalled Due to Label Mix-Up

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Recalling firmSTAQ Pharma, Inc.14135 E 42nd Ave Ste 50, N/A · Denver, CO 80239-5214

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✎ GovInfoNow plain-language explainer

What happened, in plain English

STAQ Pharma is recalling a limited number of Morphine Sulfate syringes that were incorrectly labeled as Hydro morphone. This mix-up could lead to serious medication errors if used by patients.

Why it’s dangerous

The syringes were incorrectly labeled as Morphine Sulfate when they actually contain Hydro morphone. This mix-up could lead to patients receiving the wrong medication, causing serious health issues.

Who’s affected

Patients prescribed Morphine Sulfate by a doctor who received this specific syringe model with lot number 21104221A are affected. Those using the syringes for medical purposes are at risk of medication errors.

How to tell if you have this one

Check for the lot number 21104221A on the syringe label. The product is a 25 mg/25mL Morphine Sulfate syringe in a 30 mL single-dose container.

Brand
STAQ Pharma
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Label
Verify the lot number on the syringe label; if it is 21104221A, it is part of the recall.

✎ GovInfoNow

Questions people ask

What is the specific lot number of the recalled syringes?

The recalled syringes have lot number 21104221A.

How can I tell if I have the recalled product?

Check for the lot number 21104221A on the syringe label. The product is a 25 mg/25mL Morphine Sulfate syringe in a 30 mL single-dose container.

What should I do if I have the recalled syringe?

The recall record does not specify a remedy, so contact your healthcare provider for guidance.

Take action

Contact STAQ Pharma

We’ve drafted a message you can send STAQ Pharma to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0634-2022 — STAQ Pharma STAQ Pharma

Hello,

I own a STAQ Pharma that is covered by recall D-0634-2022 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.

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Where this comes from

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.

Official source: FDA Recall #D-0634-2022 (February 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0634-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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