Kroger Specialty Pharmacy recalls Tecfidera 240mg capsules (NDC 64406-0006-02) sold between Dec 2017 and Feb 2018. Lack of processing controls may affect product safety.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Tecfidera 240mg capsules (NDC 64406-0006-02) that were dispensed from December 2017 through February 2018. This recall is due to potential processing control issues that could affect product safety.
The recall states there was a lack of processing controls, which could potentially affect the product's safety. However, the specific mechanism of how this leads to harm is not clearly described in the recall notice.
People who received Tecfidera 240mg capsules dispensed by Kroger Specialty Pharmacy between December 2017 and February 2018 are affected. Those with autoimmune conditions requiring this medication are at higher risk.
Check for Tecfidera 240mg capsules with NDC code 64406-0006-02. These were dispensed by Kroger Specialty Pharmacy between December 1, 2017, and February 12, 2018.
Look for Tecfidera 240mg capsules with NDC 64406-0006-02 dispensed between December 1, 2017, and February 12, 2018.
The recall is due to a lack of processing controls, which may affect product safety, though the specific risk is not clearly described.
Check for Tecfidera 240mg capsules with NDC 64406-0006-02 dispensed by Kroger Specialty Pharmacy between December 1, 2017, and February 12, 2018.
The recall notice does not specify a remedy, so contact Kroger Specialty Pharmacy for guidance.
We’ve drafted a message you can send Kroger Specialty Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0767-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0767-2018 from Kroger Specialty Pharmacy. 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.
