Lilly recalls Humalog KwikPen insulin pens due to potential temperature exposure during shipping. Products may be unsafe if stored outside labeled conditions. No action needed if properly stored.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Lilly has recalled Humalog KwikPen insulin pens because they may have been exposed to temperatures outside the recommended storage range during shipping. This could affect the insulin's effectiveness, but the risk is low if the pens were stored correctly after shipping.
The insulin pens may have been exposed to extreme temperatures during shipping due to weather conditions. This could potentially affect the insulin's effectiveness, but the risk is low if the pens were stored properly after shipping.
People who own or use Humalog KwikPen insulin pens from this recall. Those who have kept the pens in a cool, dry place after shipping are least at risk.
Check for the box labeled with NDC 0002-8799-59 and pens with NDC 002-7516-59. Products were sold by Lilly USA, LLC in the United States.
Ensure the pens have been stored in a cool, dry place after shipping to maintain effectiveness.
No action is needed if the pens were stored properly after shipping. The recall is for potential temperature exposure during shipping.
Check for the box labeled with NDC 0002-8799-59 and pens with NDC 002-7516-59. Products were sold by Lilly USA, LLC in the United States.
The recall is for potential temperature exposure during shipping, which could affect insulin effectiveness. However, the risk is low if the pens were stored properly after shipping.
We’ve drafted a message you can send Lilly to request your refund or repair — edit it as you like.
Subject: Recall D-0882-2022 — Lilly Lilly Hello, I own a Lilly that is covered by recall D-0882-2022 from Lilly. 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.
