Cardinal Healthcare recalls 100,000 USP units per gram Nyamyc topical cream due to temperature exposure during storage. Products may degrade if stored outside labeled conditions.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling Nyamyc topical cream because it was exposed to temperatures outside the labeled storage conditions. This could cause the product to degrade, potentially reducing effectiveness or causing safety issues.
The product was exposed to temperatures outside the labeled storage conditions during manufacturing. This could lead to degradation of the medication, potentially affecting its effectiveness or safety.
Prescription users who purchased Nyamyc topical cream from authorized sources. Those storing it in non-compliant conditions are at higher risk.
Check for Nyamyc topical cream with 100,000 USP units per gram, 60 grams, and prescription label. Products manufactured by Upsher-Smith Laboratories, Inc in Minneapolis, MN 55447 with batch number 400454.
Identify if your Nyamyc cream has 100,000 USP units per gram, 60 grams, and prescription label.
The recall indicates potential degradation due to temperature exposure, but the product may still be safe if stored correctly. Consult your healthcare provider.
Check for Nyamyc topical cream with 100,000 USP units per gram, 60 grams, prescription label, and batch number 400454 from Upsher-Smith Laboratories in Minneapolis, MN.
The recall does not specify a remedy, so contact Cardinal Healthcare for guidance on next steps.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0192-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0192-2024 from Cardinal Healthcare. 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.
