Cardinal Healthcare recalls 150mg/ml enoxaparin syringes due to potential temperature exposure during storage. This may affect product stability and safety.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling enoxap: 150mg/ml single-dose syringes with automatic safety device. The recall is because these syringes may have been exposed to temperatures outside the labeled storage conditions, which could affect product stability and safety.
The syringes were exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the risk is not severe enough to cause serious injury in normal use.
Patients prescribed enoxaparin injections and healthcare providers using these syringes are likely affected. Those who have the specific batch numbers and storage conditions may be at higher risk.
Check for the product name: Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device. Look for the batch number SAH06821A on the packaging.
Verify the batch number on the syringe packaging; the affected batch is SAH06821A.
The products were exposed to temperatures outside the labeled storage conditions during manufacturing, which could affect product stability and safety.
The official recall notice does not specify a remedy or action for affected products.
Check for the batch number SAH06821A on the packaging of the Enoxaparin Sodium Injection syringes.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0179-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0179-2024 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.
