Kroger Specialty Pharmacy recalls Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28-day supply manufactured between Dec 2017 and Feb 2018 due to lack of processing controls.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28-day supply because of a lack of processing controls. This recall affects patients who received this specific product between December 2017 and February 2018. The issue could lead to incorrect dosing if the product is used without proper handling.
The recall is due to a lack of processing controls, which could result in incorrect dosing if the product is not handled properly. This issue may lead to underdosing or overdosing depending on how the product is administered.
Patients who received the Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28-day supply between December 2017 and February 2018 are affected. Those with multiple doses of this product are at higher risk due to potential dosing errors.
Check for the product name 'Avonex 30 mcg/0.5 mL PFS Kit' with NDC code 59627-0222-05. The product was dispensed between December 1, 2017, and February 12, 2018.
Verify the NDC code 59627-0222-05 and dispensing dates (Dec 2017 to Feb 2018) to confirm if your product is affected.
The recall states there is a lack of processing controls, which could lead to incorrect dosing. The product may not be safe to use without proper handling.
Check for the NDC code 59627-0222-05 and dispensing dates between December 1, 2017, and February 12, 2018.
The recall does not specify a remedy, so contact Kroger Specialty Pharmacy directly 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-0776-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0776-2018 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.
