American Health Packaging recalls Nitrofurantoin Capsules due to dissolution failure at 0-time. This may affect drug effectiveness. Check product details to see if you have the recalled batch.
Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
American Health Packaging is recalling Nitrofurantoin Capsules because they failed to dissolve properly at the time of repackaging. This could mean the medication doesn't work as intended when taken.
The capsules failed to dissolve properly at the time of repackaging, which means the medication might not release correctly in the body. This could lead to reduced effectiveness of the drug for treating urinary tract infections.
People who have the specific Nitrofurantoin Capsules with NDC 68084-446-11 and Lot # 1003829 are affected. Those taking the medication for urinary tract infections may be at risk if the capsules don't dissolve correctly.
Check for Nitrofurantoin Capsules with NDC 68084-446-11 and Lot # 1003829. The product comes in 10-count blisters per card, 10 cards per carton, and is only available by prescription.
Identify if your Nitrofurantoin Capsules have NDC 68084-446-11 and Lot # 1003829.
The capsules failed to dissolve properly at the time of repackaging, which could mean the medication doesn't work as intended.
Look for Nitrofurantoin Capsules with NDC 68084-446-11 and Lot # 1003829, which come in 10-count blisters per card, 10 cards per carton, and are only available by prescription.
The recall record does not specify a remedy, so you should check with your healthcare provider or pharmacist for guidance.
We’ve drafted a message you can send American Health Packaging to request your refund or repair — edit it as you like.
Subject: Recall D-0880-2022 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-0880-2022 from American Health Packaging. 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.
