Kroger Specialty Pharmacy recalls Revlimid 5mg oral capsules (NDC 59572-0405-28) due to lack of processing controls. Affected units dispensed between Dec 2017 and Feb 2018.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Revlimid 5mg oral capsules (NDC 59572-0405-28) because of insufficient processing controls. This could lead to medication errors or incorrect dosing if the product is used without proper quality checks.
The recall is due to a lack of processing controls, which could result in medication errors or incorrect dosing. This means the product might not be manufactured to the required quality standards, potentially causing harm if used without proper verification.
Patients prescribed Revlimid 5mg capsules by Kroger Specialty Pharmacy between December 2017 and February 2018 are affected. Those using the product without proper quality checks may be at higher risk.
Check for the product name 'Revlimid 5mg oral cap' with NDC code 59572-0405-28. The product was dispensed between December 1, 2017, and February 12, 2018.
Verify the NDC code 59572-0405-28 and dispensing dates between December 1, 2017, and February 12, 2018.
The recall is due to lack of processing controls, which could lead to medication errors. The official notice does not specify if this causes serious injury.
Check for Revlimid 5mg oral capsules with NDC 59572-0405-28 dispensed between December 1, 2017, and February 12, 2018.
The recall 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-0774-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0774-2018 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.
