Pine Pharmaceuticals recalls specific lidocaine-phenylephrine vials due to lack of sterility assurance. Affected lots expire by 2024; contact for details.
Lack of Assurance of Sterility
Pine Pharmaceuticals is recalling certain compounded lidocaine-phenylephrine vials that may not be sterile. This could lead to infections if used improperly. Affected vials have specific lot numbers and expiration dates.
The vials lack assurance of sterility, meaning they might contain harmful bacteria or contaminants. If used for medical purposes, this could cause infections or other health issues.
Prescription users of compounded lidocaine-phenylephrine vials from Pine Pharmaceuticals in Tonawanda, NY. Those with the listed lot numbers and expiration dates are most at risk.
Check the vial label for lot numbers 67849, 67887, 68260, 68534, 68816, 69046, or 69971. These vials expire by October 2023 through January 2024.
Look for lot numbers 67849, 67887, 68260, 68534, 68816, 69046, or 69971 on the vial.
The vials lack assurance of sterility, which could lead to infections if used improperly.
Check the vial label for lot numbers 67849, 67887, 68260, 68534, 68816, 69046, or 69971.
The recall record does not specify a remedy, so contact Pine Pharmaceuticals for guidance.
We’ve drafted a message you can send Pine Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0059-2024 — Pine Pharmaceuticals Pine Pharmaceuticals Hello, I own a Pine Pharmaceuticals that is covered by recall D-0059-2024 from Pine Pharmaceuticals. 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.
