STAQ Pharma recalls 10mg/50mL Hydromorphone IV injection due to missing lot and expiry dates on labels. This could lead to medication errors if the correct batch is not identified.
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma is recalling a specific IV injection product because its labels lack proper lot and expiration dates. This risk could cause medication errors if healthcare providers use the wrong batch.
The injection product has incorrect or missing lot and expiration dates on its label. This could lead to medication errors if healthcare providers use the wrong batch of the drug.
Healthcare providers using this IV injection for medical procedures. Those most at risk are medical staff handling the product without verified labeling.
Check for the lot number 25104595A and expiry date 27DEC2025 on the label. This product was sold by STAQ Pharma Inc. in Denver, Colorado.
Verify the lot number 25104595A and expiry date 27DEC2025 on the product label.
The product has incorrect or missing lot and expiration dates on its label, which could lead to medication errors.
Look for the lot number 25104595A and expiry date 27DEC2025 on the label. This product was sold by STAQ Pharma Inc. in Denver, Colorado.
Check the label for the lot number and expiry date. If the labels are missing or incorrect, contact STAQ Pharma for further instructions.
We’ve drafted a message you can send STAQ Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0023-2026 — STAQ Pharma STAQ Pharma Hello, I own a STAQ Pharma that is covered by recall D-0023-2026 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.
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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.
