Kroger Specialty Pharmacy recalls Kisqali 200mg 63-tablet supply with NDC 00078-0874-63 due to lack of processing controls. Affected units dispensed between Dec 2017 and Feb 2018.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Kisqali 200mg 63-tablet supplies (NDC 00078-0874-63) that were dispensed between December 2017 and February 2018. This recall is due to a lack of processing controls, which may pose a risk to patients using the medication.
The recall is due to a lack of processing controls during manufacturing. This could lead to medication errors or inconsistencies in the product, potentially affecting patient safety.
Patients who received the Kisqali 200mg 63-tablet supply (NDC 00078-0874-63) dispensed between December 2017 and February 2018 are affected. Those with a prescription for this medication are most at risk.
Check for the product name 'Kisqali 200mg 63-tablet' with NDC code 00078-0874-63. The affected units were dispensed between December 1, 2017, and February 12, 2018.
Look for the NDC code 00078-0874-63 on the product label to confirm if it's affected.
The recall is due to a lack of processing controls, which may pose a risk. Patients should not use the affected product without consulting their healthcare provider.
Check the NDC code on the product label. If it matches 00078-0874-63 and was dispensed between December 2017 and February 2018, contact Kroger Specialty Pharmacy for guidance.
The recall record does not specify a replacement process. Contact Kroger Specialty Pharmacy directly for assistance.
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-0799-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0799-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
