Pfizer recalls Accure: 20mg/12.5mg tablets with potential impurities above safe levels. Rx-only medication distributed by Parke-Davis in Germany. Check NDC 0071-5212-23 and lot FG5381 for affected units.
CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Pfizer is recalling Accuretic (quinapril HCl/hydrochlorothiazide) tablets due to impurities that may exceed safe levels. This is a prescription-only medication distributed in Germany with a specific lot number and expiration date.
The tablets contain N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurities that could exceed the acceptable daily intake limit. This means the medication might have unsafe levels of these impurities, though the exact risk is not specified.
Prescription patients who have the specific Accuretic tablets with NDC 0071-5212-23 and lot FG5381. Those with the medication may be at risk if the impurities exceed safe limits.
Check for the NDC code 0071-5212-23 and lot number FG5381 on the packaging. The medication was made in Germany and expires in August 2024.
Look for the NDC code 0071-5212-23 and lot number FG5381 on the packaging to confirm if it's affected.
The recall states there may be impurities above safe limits, but the exact risk is not specified. Consult your doctor for advice.
The recall does not specify a remedy, so contact your doctor for guidance on whether to stop using the medication.
Check the NDC code 0071-5212-23 and lot number FG5381 on the packaging. The medication was made in Germany and expires in August 2024.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0761-2022 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0761-2022 from Pfizer. 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.
