Advanced Pharma Inc. recalls HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use
Advanced Pharma recalls hydromorphone 20 mg/100 mL injectable solution with sub-potency risk. This may not provide intended pain relief. Consumers should contact the manufacturer for details.
Lower-risk recall
Sub-potency
Contact the company & request your remedy
What happened, in plain English
Advanced Pharma is recalling hydromorphone 20 mg/100 mL injectable solution because it may be sub-potency. This means the medication might not work as intended for pain relief. If you have this product, contact the manufacturer for guidance. Read more at govinfonow.com/recall/38872-advanced-pharma-recalls-hydromorphone-injectable-solution-due-to-sub-potency.
Source Summary by GovInfoNow · govinfonow.com/recall/38872-advanced-pharma-recalls-hydromorphone-injectable-solution-due-to-sub-potency · Updated October 5, 2026 · FDA enforcement record: FDA #D-1251-2019
Cite this page
“Advanced Pharma recalls hydromorphone injectable solution due to sub-potency.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38872-advanced-pharma-recalls-hydromorphone-injectable-solution-due-to-sub-potency. Based on FDA recall #D-1251-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1251-2019%22&limit=1).
Why it’s dangerous
Sub-potency means the medication may not contain enough active ingredient to provide the intended pain relief. This could lead to inadequate pain management if the product is used as directed. However, the product is not dangerous in the sense of causing injury or death.
Who’s affected
People who have the hydromorphone 20 mg/100 mL injectable solution from Advanced Pharma. Those using this medication for pain relief are most at risk of not getting adequate pain management.
How to tell if you have this one
Look for the product name: 'Hydro morphone 20 mg/100 mL Injectable Solution'. Check the lot number on the label: 01/14/19 0215 22110P, with an expiration date of 04/29/2019.
- Brand
Advanced Pharma- Category
Drug
What to do — step by step
Contact Manufacturer
Reach out to Advanced Pharma at (877) 794-0404 for specific guidance on this recall.
Questions people ask
Is this product dangerous?
No, the recall is for sub-potency, which means it may not work as intended for pain relief, but it does not pose a risk of injury or death.
How can I tell if I have the recalled product?
Check the label for the lot number 01/14/19 0215 22110P and expiration date 04/29/2019 on the hydromorphone 20 mg/100 mL injectable solution.
What should I do if I have this product?
Contact Advanced Pharma at (877) 794-0404 for specific guidance on this recall.
Contact Advanced Pharma
We’ve drafted a message you can send Advanced Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-1251-2019 — Advanced Pharma Advanced Pharma Hello, I own a Advanced Pharma that is covered by recall D-1251-2019 from Advanced 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-1251-2019 (April 26, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1251-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.