Macleods Pharma recalls 10mg Rizatriptan Benzoate orally disintegrating tablets due to organic impurities found in lab tests. This prescription medication is not safe for use.
Out-of-specification test results obtained in Organic Impurities test during analysis of controlled samples.
Macleods Pharma is recalling 10mg Rizatriptan Benzoate orally disintegrating tablets because lab tests found organic impurities. This means the medication may not be safe for use as prescribed.
The lab tests found organic impurities in the medication. This could mean the tablets are unsafe for use, but the specific health risk is not clearly stated in the recall notice.
Prescription patients who received the recalled tablets from Macleods Pharma. Those with headaches needing treatment are most at risk.
Check for the product name 'Rizatriptan Benzoate Orally Disintegrating Tablets 10mg', 18 tablets in blister packs, with NDC 33342-094-41 and lots BRM2111A through BRM2116A.
Look for the NDC code 33342-094-41 and lots BRM2111A through BRM2116A on the blister pack.
The recall is due to organic impurities found in lab tests, which may make the medication unsafe.
The recall notice does not specify a remedy, so contact your doctor or pharmacist for advice.
The recall notice does not describe a specific health risk, so the risk level is unknown.
We’ve drafted a message you can send Macleods Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0080-2022 — Macleods Pharma Macleods Pharma Hello, I own a Macleods Pharma that is covered by recall D-0080-2022 from Macleods Pharma. 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.