Macleods Pharma Usa Inc recalls Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc.,
Macleods Pharma recalls 15mg Pioglit: Superpotent risk in 30-count bottles. Rx only. Check NDC 33342-054-07 and lot BPF901A.
Recall notice
Superpotent
Contact the company & request your remedy
What happened, in plain English
Macleods Pharma recalls 15mg Pioglitazone Hydrochloride Tablets (30-count bottles) due to a superpotent risk. This is a prescription-only medication that could pose serious health risks if misused. Read more at govinfonow.com/recall/37915-macleods-pioglitazone-tablets-15mg-recall-superpotent-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37915-macleods-pioglitazone-tablets-15mg-recall-superpotent-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0140-2020
Cite this page
“Macleods Pioglitazone Tablets 15mg Recall: Superpotent Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37915-macleods-pioglitazone-tablets-15mg-recall-superpotent-risk. Based on FDA recall #D-0140-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0140-2020%22&limit=1).
Why it’s dangerous
The product is labeled 'superpotent,' meaning it could cause severe health effects if taken inappropriately. This risk is specific to the medication's potency and requires careful medical supervision.
Who’s affected
Prescription patients using the recalled 15mg Pioglitazone tablets. Those with diabetes who require this medication are most at risk.
How to tell if you have this one
Check for 30-count bottles labeled 'Pioglitazone Hydrochloride Tablets USP 15 mg.' Look for NDC code 33342-054-07 and lot number BPF901A.
- Brand
Macleods- Category
Drug
What to do — step by step
Check Product Details
Identify the NDC code 33342-054-07 and lot number BPF901A on the bottle.
Questions people ask
Is this product safe to use?
The recall states it has a 'superpotent' risk, but no specific safety details are provided in the official notice.
What should I do if I have this product?
The official notice does not specify a remedy, so no action is required beyond checking the product details.
How can I confirm if my product is recalled?
Check for NDC code 33342-054-07 and lot number BPF901A on the bottle label.
Contact Macleods
We’ve drafted a message you can send Macleods to request your refund or repair — edit it as you like.
Subject: Recall D-0140-2020 — Macleods Macleods Hello, I own a Macleods that is covered by recall D-0140-2020 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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Where this comes from
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.
- Official source: FDA Recall #D-0140-2020 (September 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0140-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.