Kroger Specialty Pharmacy recalls Xalkori 250mg capsules (NDC 00069-8140-20) with potential processing control issues. Affected units dispensed between Dec 2017 and Feb 2018.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Xalkori 250mg capsules (NDC 00069-8140-20) because of lack of processing controls. This could lead to medication errors or improper dosing if the product is used without proper quality checks.
The lack of processing controls means the medication may not be handled or dispensed correctly, potentially leading to incorrect dosing or medication errors. This could affect the safety and effectiveness of the treatment.
Patients prescribed Xalkori 250mg capsules with the specific NDC code 00069-8140-20 who received the product between December 2017 and February 2018 are affected. Those with the medication dispensed during this timeframe are most at risk.
Check for the NDC code 00069-8140-20 on the product label. The capsules were dispensed between December 1, 2017, and February 12, 2018.
Look for the NDC code 00069-8140-20 on the Xalkori 250mg capsule packaging.
The recall is due to lack of processing controls, which could lead to medication errors. However, the risk level is low as the product was dispensed within a specific timeframe and the hazard does not cause immediate serious injury.
Check the product label for NDC code 00069-8140-20. The capsules were dispensed between December 1, 2017, and February 12, 2018.
The recall does not specify a remedy, so contact your pharmacy or healthcare provider for guidance on next steps.
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-0779-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0779-2018 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.
