Athenex Pharma recalls 20mg Phenylephrine HCl injection in 0.9% saline due to defective container. This may cause injury if the container breaks during use. Contact Athenex for details.
Defective container
Athenex Pharma is recalling phenylephrine injections that come in 250mL bags. The container may be defective and break during use, potentially causing injury.
The container may break during use, which could lead to injury. This is a defect in the packaging that affects the product's safety.
Prescription users of phenylephrine injections for medical purposes. Patients using the recalled product are at risk if the container breaks.
Check for the product name 'Phenylephrine HCl Injection in 0.9% Sodium Chloride, 20 mg, 250 mL'. Look for lot numbers F2101654 (exp 5/30/22), F2101834 (exp 7/03/22), or F2200110 (exp 7/27/22).
Look for the lot numbers F2101654 (exp 5/30/22), F2101834 (exp 7/03/22), or F2200110 (exp 7/27/22) on the container.
The product is recalled due to a defective container that may break during use, so it is not safe to use.
The official recall notice does not specify a remedy, so contact Athenex Pharma Solutions for further instructions.
Check for the lot numbers F2101654 (exp 5/30/22), F2101834 (exp 7/03/22), or F2200110 (exp 7/27/22) on the container.
We’ve drafted a message you can send Athenex to request your refund or repair — edit it as you like.
Subject: Recall D-0711-2022 — Athenex Athenex Hello, I own a Athenex that is covered by recall D-0711-2022 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.
