Cardinal Health dba Specialty Pharmaceutical Services recalls Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose, For subcutaneous use only, Rx Only,
Cardinal Health recalls Nucala (mepolizumab) injections due to temperature abuse. Product must be stored within labeled requirements to prevent safety issues.
Lower-risk recall
Temperature Abuse; Product stored and shipped outside of labeled storage requirements.
Contact the company & request your remedy
What happened, in plain English
Cardinal Health is recalling Nucala injections because they were stored or shipped outside the required temperature range. This could lead to product instability and potential safety risks if used improperly. Read more at govinfonow.com/recall/38024-nucala-injection-recall-temperature-abuse-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/38024-nucala-injection-recall-temperature-abuse-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1876-2019
Cite this page
“Nucala Injection Recall: Temperature Abuse Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38024-nucala-injection-recall-temperature-abuse-risk. Based on FDA recall #D-1876-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1876-2019%22&limit=1).
Why it’s dangerous
The product was stored or shipped outside the labeled temperature requirements. This could cause the medication to become unstable, potentially affecting its safety and effectiveness.
Who’s affected
People with prescriptions for Nucala injections who received the recalled product. Those with specific storage conditions not met are at higher risk.
How to tell if you have this one
Check for the product name 'Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose'. Look for lot number S25X with expiration date 03/31/21.
- Brand
Cardinal Health- Category
Drug
What to do — step by step
Check Storage Conditions
Ensure the product is stored within the labeled temperature requirements to maintain stability.
Questions people ask
Is this product safe to use?
The product may be unsafe if stored or shipped outside the labeled temperature requirements. Check your storage conditions.
How do I know if I have the recalled product?
Look for the product name 'Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose' with lot number S25X and expiration date 03/31/21.
What should I do if I have the recalled product?
Ensure the product is stored within the labeled temperature requirements to maintain stability. Contact your healthcare provider for further guidance.
Contact Cardinal Health
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall D-1876-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall D-1876-2019 from Cardinal Health. 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-1876-2019 (September 6, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1876-2019 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.