Aurobindo Pharma recalls 45mg Pioglitazone tablets with failed specifications that may be superpotent. Consumers should check NDC 57237-221-05 and batch numbers PF4520028A/B for affected products.
Superpotent and Failed Tablet/Capsule Specifications
Aurobindo Pharma is recalling 45mg Pioglitazone tablets that may have failed specifications, making them superpotent. This could cause harmful effects if taken as directed.
The tablets may have failed specifications, meaning they could be superpotent. This could lead to harmful effects if taken as directed, potentially causing serious health issues.
People who own or use the recalled 45mg Pioglitazone tablets with NDC 57237-221-05 and batch numbers PF4520028A or PF4520028B are affected. Those taking the medication for diabetes are most at risk.
Check for NDC 57237-221-05 on the product label. The batch numbers are PF4520028A or PF4520028B with an expiration date of November 2022.
Look for NDC 57237-221-05 and batch numbers PF4520028A or PF4520028B on the tablet packaging.
The batch numbers are PF4520028A and PF4520028B.
Check for NDC 57237-221-05 and batch numbers PF4520028A or PF4520028B on the tablet packaging.
The recall does not specify a remedy, so there is no instruction to stop using the tablets.
We’ve drafted a message you can send Aurobindo Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0450-2022 — Aurobindo Pharma Aurobindo Pharma Hello, I own a Aurobindo Pharma that is covered by recall D-0450-2022 from Aurobindo 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.
