Macleods Pharma USA recalls 1000-count losartan/hydrochlorothiazide tablets (Rx only) due to plastic-like foreign substance. Consumers should check NDC 33342-050-44 and lot number BLK2304A.
Presence of foreign substance: plastic-like substance.
Macleods Pharma recalled 1000-count losartan and hydrochlorothiazide tablets (Rx only) because they contain a plastic-like foreign substance. This could cause harm if ingested, so affected users should stop using the product and contact their pharmacy.
The tablets contain a plastic-like foreign substance that could be ingested and cause harm. This is a serious hazard because the foreign material might lead to injury or health issues if taken.
Prescription users of losartan and hydrochlorothiazide tablets who purchased the 1000-count bottle with NDC 33342-050-44 and lot number BLK2304A. People with high blood pressure or kidney issues are at higher risk.
Check for the NDC code 33342-050-44 and lot number BLK2304A on the product label. The product is a 1000-count bottle of losartan/hydrochlorothiazide tablets (Rx only) manufactured by Macleods Pharma USA.
Immediately stop using the recalled tablets and contact your pharmacy for instructions.
The recalled product is a 1000-count bottle of losartan potassium and hydrochlorothiazide tablets (50mg/12.5mg) with NDC 33342-050-44 and lot number BLK2304A.
Check the product label for NDC 33342-050-44 and lot number BLK2304A. The product is a prescription-only 1000-count bottle.
Stop using the product immediately and contact your pharmacy for instructions.
We’ve drafted a message you can send Macleods Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0498-2024 — Macleods Pharma Macleods Pharma Hello, I own a Macleods Pharma that is covered by recall D-0498-2024 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.
