Cardinal Healthcare recalls amoxicillin oral suspension due to potential temperature exposure during storage. Products may be affected if stored outside labeled conditions. Check NDC 0093-4161-73 batch 35447184A for affected items.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling amoxicillin oral suspension that may have been exposed to temperatures outside the labeled storage conditions. This could affect product stability and safety, but the recall does not specify a risk of serious injury or illness.
The amoxicillin suspension was exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the product's stability and effectiveness, but the recall does not indicate a risk of serious injury or illness.
People who own or use the recalled amoxicillin suspension, particularly those in Canada or the U.S. who purchased it from the manufacturer or authorized distributors. Those with specific medical conditions requiring precise medication dosing may be at slightly higher risk.
Check for the product name 'AMOXICILLIN for Oral Suspension USP, 400MG/5ML, 100ML (when reconstituted)' with NDC code 0093-4161-73 and batch number 35447184A. The product was manufactured in Canada by TEVA CANA and distributed by TEVA PHARMACEUTICALS USA.
Identify the NDC code 0093-4161-73 and batch number 35447184A on the product label.
The recall states the product may have been exposed to temperatures outside labeled storage conditions, but it does not specify a risk of serious injury or illness.
Check for the NDC code 0093-4161-73 and batch number 35447184A on the product label.
The recall does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0165-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0165-2024 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.
