Athenex Pharma recalls 8mg epinephrine injections with defective containers. This may cause injury during use. Contact for return instructions.
Defective container
Athenex Pharma recalls epinephrine injections that may have defective containers. This could lead to injury if the container fails during use.
The container may be defective, potentially causing injury if it fails during use. This is a serious hazard for medical emergencies.
People with prescriptions for epinephrine injections from Athenex Pharma. Those using the product for medical emergencies are at higher risk.
Check for the product name 'Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride', brand 'Athenex Pharma', and lot numbers F2101780 or F2101781.
Look for lot numbers F2101780 or F2101781 on the container.
The recall states the container may be defective, so it is not safe to use.
Check for lot numbers F2101780 or F2101781 on the container.
The recall does not specify a remedy, so contact Athenex Pharma for instructions.
We’ve drafted a message you can send Athenex to request your refund or repair — edit it as you like.
Subject: Recall D-0712-2022 — Athenex Athenex Hello, I own a Athenex that is covered by recall D-0712-2022 from Athenex. 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.
