Cardinal Healthcare recalls 100mg doxycycline capsules due to potential temperature exposure during storage. This may affect product stability and safety. Learn if your product is affected and what to do.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling doxycycline capsules that may have been exposed to temperatures outside their labeled storage conditions. This could affect product stability and safety, though the recall does not specify a risk of serious injury.
The capsules may have been exposed to temperatures outside the labeled storage conditions during manufacturing or distribution. This could potentially affect product stability and safety, though the recall does not specify a risk of serious injury.
Prescription holders of doxycycline capsules with NDC 68180-652-08 and batch G104819. Patients who store these capsules in temperatures outside the labeled range are most at risk.
Check for the NDC code 68180-652-08 and batch number G104819 on the packaging. The capsules are prescription-only doxycycline 100mg, 50-count.
Look for the NDC code 68180-652-08 and batch number G104819 on the packaging.
The recall does not specify a risk of serious injury, but the capsules may have been exposed to temperatures outside the labeled storage conditions, potentially affecting product stability and safety.
Check for the NDC code 68180-652-08 and batch number G104819 on the packaging. The capsules are prescription-only doxycycline 100mg, 50-count.
The recall does not specify a remedy, so no action is required beyond checking if your product matches the description.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0178-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0178-2024 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.
