Pine Pharmaceuticals recalls specific lots of compounded Cefuroxime 4mg/0.4mL syringes due to lack of sterility assurance. Affected patients should contact their healthcare provider for guidance.
Lack of Assurance of Sterility
Pine Pharmaceuticals has recalled certain compounded Cefuroxime 4mg/0.4mL syringes because they may not be sterile. This could lead to infections if used improperly. Patients should not use these syringes and contact their healthcare provider.
The syringes may not be sterile, which could cause infections if used for injections. This is a serious risk because infections can lead to complications like sepsis or other health issues.
Patients who received the recalled syringes from Pine Pharmaceuticals' compounded batches. Healthcare providers who dispensed these syringes are most at risk.
Check the lot number on the syringe label: 67918 through 71068. These syringes were compounded by Pine Pharmaceuticals at 355 Riverwalk Parkway, Tonawanda, NY.
Immediately stop using the recalled syringes as they may not be sterile.
The recall is due to a lack of assurance of sterility, which could lead to infections if the syringe is used.
Check the lot number on the syringe label: 67918 through 71068. These syringes were compounded by Pine Pharmaceuticals at 355 Riverwalk Parkway, Tonawanda, NY.
Immediately stop using the syringe and contact your healthcare provider 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-0057-2024 — Pine Pharmaceuticals Pine Pharmaceuticals Hello, I own a Pine Pharmaceuticals that is covered by recall D-0057-2024 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.
