Eli Lilly recalls Trulicity 1.5mg/0.5mL pens due to temperature exposure during shipping. Products may be unstable if stored outside labeled conditions. Check NDC 00002-1434-80 and lot D482749A.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.
Eli Lilly is recalling Trulicity (dulaglutide) injections that may have been exposed to improper temperatures during shipping. This could affect product stability and safety, but the recall does not require immediate action beyond checking the product details.
The product was exposed to temperatures outside the labeled storage conditions during shipping due to weather conditions. This could potentially affect the stability of the medication, though the recall does not indicate immediate harm to users.
People with prescriptions for Trulicity injections who received the specific lot number D482749A (expiring 10/15/2023) are affected. Those who stored the pens outside recommended temperature ranges during shipping may be at slightly higher risk.
Check for the NDC code 00002-1434-80 and lot number D482749A on the pen packaging. The product expires 10/15/2023 and is only available by prescription.
Verify the NDC code 00002-1434-80 and lot number D482749A on the pen packaging.
No, the recall does not require immediate action. Check the product details to see if you have the specific lot number.
The recall does not require discarding or returning the pens. Check the product details to confirm if you have the specific lot number.
The recall indicates a potential stability issue from temperature exposure, but no serious injury risk is mentioned.
We’ve drafted a message you can send Eli Lilly to request your refund or repair — edit it as you like.
Subject: Recall D-0883-2022 — Eli Lilly Eli Lilly Hello, I own a Eli Lilly that is covered by recall D-0883-2022 from Eli 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.
