Mylan recalls 20mg esomeprazole capsules due to impurities detected in lab tests. These capsules may cause serious health issues if taken. Consumers should contact Mylan for details.
Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Mylan is recalling 20mg esomeprazole magnesium delayed-release capsules that failed lab tests for impurities. This could pose serious health risks if taken as directed.
The capsules failed lab tests for impurities at room temperature. This means the medication may contain harmful substances that could cause serious health problems if taken.
People who have the specific lot numbers listed in the recall notice. Those taking this medication for acid reflux or ulcers are most at risk.
Check the blister pack for the lot numbers: 3112743 (exp. 4/30/2023), 3112582 (exp. 3/31/2023), or 3110438/3111708/3111120 (exp. 7/31/2022).
Look for the lot numbers listed in the recall notice: 3112743, 3112582, or 3110438/3111708/3111120.
The capsules failed lab tests for impurities at room temperature, which could pose serious health risks if taken.
Contact Mylan directly for instructions on what to do with the recalled capsules.
The recall notice states that the capsules may contain harmful impurities that could cause serious health issues.
We’ve drafted a message you can send Mylan to request your refund or repair — edit it as you like.
Subject: Recall D-0860-2022 — Mylan Mylan Hello, I own a Mylan that is covered by recall D-0860-2022 from Mylan. 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.
