Pine Pharmaceuticals recalls Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection due to lack of sterility assurance. This affects compounded vials with lot #69985 expiring 11/15/2023. No remedy is specified in the recall notice.
Lack of Assurance of Sterility
Pine Pharmaceuticals has recalled a compounded vancomycin solution for eye injections because it may not be sterile. This poses a risk of infection if used improperly. The recall affects specific vials with lot number 69985 that expired by November 15, 2023.
The solution may not be sterile, which can lead to infections in the eye during injection. This is a serious risk because eye infections can cause vision damage or other complications if the medication is not properly sterilized.
Healthcare professionals who compounded this vancomycin solution for eye injections are likely affected. Patients receiving the compounded medication from this source are at risk if the solution was not sterile.
Check for the vial label that says 'Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection, 0.8 ML Single Dose Vial, Rx only, Compounded by: Pine Pharmaceuticals'. Look for lot number 69985 with an expiration date of November 15, 2023.
Look for the label indicating 'Vancomycin 1 MG/0.1 ML Solution for Intraocular Injection, 0.8 ML Single Dose Vial, Rx only, Compounded by: Pine Pharmaceuticals'.
The recall notice does not specify any remedy.
The recalled vials have an expiration date of November 15, 2023.
Check the vial label for the product name and lot number 69985.
We’ve drafted a message you can send Pine Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0051-2024 — Pine Pharmaceuticals Pine Pharmaceuticals Hello, I own a Pine Pharmaceuticals that is covered by recall D-0051-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
