Macleods Pharmaceuticals recalls 2.5 mg Olanzapine tablets due to failed impurities and degradation specifications. This prescription medication may pose health risks if used as intended.
Failed Impurities/Degradation Specifications
Macleods Pharmaceuticals is recalling 2.5 mg Olanzapine tablets that may contain impurities or degrade improperly. This could lead to health risks if taken as prescribed.
The tablets failed impurities and degradation specifications, meaning they may contain harmful substances or break down in a way that could affect safety. This could lead to health risks if taken as intended.
Prescription patients who have received the specific Olanzapine tablets with NDC 33342-067-07 and lot number BOB12318A. Those with the medication in their possession are most at risk.
Check for the product name 'Olanzapine Tablets, USP 2.5 mg, 30-count bottle', prescription-only, and lot number BOB12318A. The NDC code is 33342-067-07.
Look for the lot number BOB12318A and NDC 33342-067-07 on the product label.
The recall states the tablets failed impurities and degradation specifications, but does not specify if they are safe to take. Consult your healthcare provider for advice.
Check for the lot number BOB12318A and NDC 33342-067-07 on the product label.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Macleods to request your refund or repair — edit it as you like.
Subject: Recall D-0154-2025 — Macleods Macleods Hello, I own a Macleods that is covered by recall D-0154-2025 from Macleods. 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.
