Central Admixture Pharmacy Services recalls phenylephrine syringes with specific lot numbers due to lack of sterility assurance. Consumers should contact the manufacturer for details on affected products and remedies.
Lack of assurance of sterility:
Central Admixture Pharmacy Services has recalled phenylephrine syringes that may not be sterile. This could lead to infections if used improperly. Affected products have specific lot numbers and expiration dates.
The syringes lack assurance of sterility, meaning they could be contaminated with bacteria. If used, this could cause infections, especially in medical settings where sterile products are critical.
Individuals who have received a prescription for phenylephrine syringes with the listed lot numbers and expiration dates are affected. Healthcare providers and patients using these syringes are at risk.
Check the lot numbers on the syringe: 17-275323, 17-275345, 17-275642, 17-275643, 17-275671, 17-275675, 17-275677, 17-276188. Also check the expiration dates: October 3, 2023, October 8, 2023, October 9, 2023, and October 18, 2023.
Identify the lot numbers and expiration dates on the syringe to determine if it is affected.
The recalled product is phenylephrine in 0.9 sodium chloride, 800 mcg/10 mL, 10 mL syringe, prescription-only, with specific lot numbers and expiration dates.
The recall record does not specify a remedy, so contact Central Admixture Pharmacy Services for further instructions.
Check the lot numbers: 17-275323, 17-275345, 17-275642, 17-275643, 17-275671, 17-275675, 17-275677, 17-276188. Also check the expiration dates: October 3, 2023, October 8, 2023, October 9, 2023, and October 18, 2023.
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-0006-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0006-2024 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.
