Kroger Specialty Pharmacy recalls Letrozole 2.5 mg tabs (NDC 51991-0759-33) due to lack of processing controls. All lots dispensed between Dec 2017 and Feb 2018 are affected.
Lack of Processing Controls.
Kroger Specialty Pharmacy is recalling Letrozole 2.5 mg tablets (NDC 51991-0759-33) because of a lack of processing controls. This could lead to medication errors or incorrect dosing if the product is used without proper quality checks.
The lack of processing controls means the medication may not be handled or checked properly during manufacturing, potentially leading to incorrect dosing or medication errors. This could affect the safety and effectiveness of the drug.
People who received Letrozole 2.5 mg tablets from Kroger Specialty Pharmacy between December 2017 and February 2018 are affected. Those with a prescription for this medication are most at risk.
Check for the product name 'Letrozole 2.5 mg tab' with NDC code 51991-0759-33. The product was dispensed by Kroger Specialty Pharmacy between December 1, 2017, and February 12, 2018.
Verify the NDC code 51991-0759-33 and the dispensing dates (Dec 1, 2017 - Feb 12, 2018) to confirm if your product is affected.
The recall is due to a lack of processing controls, which could lead to medication errors. However, the hazard level is low risk as the remedy does not require immediate action.
Check for the NDC code 51991-0759-33 and confirm the dispensing dates were between December 1, 2017, and February 12, 2018.
The recall does not specify a remedy, so you should check with Kroger Specialty Pharmacy for further instructions.
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-0794-2018 — Kroger Specialty Pharmacy Kroger Specialty Pharmacy Hello, I own a Kroger Specialty Pharmacy that is covered by recall D-0794-2018 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.
