Central Admixture Pharmacy Services recalls phenylephrine in 0.9% sodium chloride syringes (NDC 71286-6009-1) due to lack of sterility assurance. Affected lots expire through October 2023.
Lack of assurance of sterility:
Central Admixture Pharmacy Services is recalling phenylephrine syringes that may not be sterile. This could lead to infections if used in medical procedures. Patients and healthcare providers should check their lot numbers and contact the manufacturer if they have the affected products.
The syringes may not be sterile, which could cause infections if used in medical procedures. This is a serious concern for healthcare settings where the product is administered directly to patients.
Healthcare providers and patients using the recalled phenylephrine syringes for medical procedures. Those with the specific lot numbers listed in the recall are most at risk.
Check the lot numbers on the syringe: 17-275152 through 17-275984. The product expires between October 1 and October 18, 2023. The NDC code is 71286-6009-1.
Look for the lot numbers listed in the recall: 17-275152 through 17-275984.
Reach out to Central Admixture Pharmacy Services, Inc. at 7935 Dunbrook Road, Suite C, San Diego, CA 92126 for further assistance.
Phenylephrine in 0.9% sodium chloride, 1,000 mcg/10 mL syringes (NDC 71286-6009-1) for medical use.
Lot numbers 17-275152 through 17-275984, expiring between October 1 and October 18, 2023.
Check the lot number on the syringe; affected lots are listed in the recall as 17-275152 through 17-275984.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0007-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0007-2024 from Central Admixture Pharmacy Services. 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.
