Central Admixture Pharmacy Services recalls phenylephrine syringes (NDC 72196-6009-1) with potential sterility issues. These are prescription-only syringes sold in specific lots and expiration dates. Consumers should check their product details to determine if affected.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled phenylephrine syringes (1,000 mcg/10mL) due to a lack of assurance of sterility. This means the syringes could be contaminated, posing a risk of infection if used for medical purposes.
The syringes lack validation data for decontamination cycles, meaning they may not be sterile. This could lead to infections if the syringes are used for medical procedures without proper sterilization.
Prescription patients using phenylephrine syringes for medical purposes. Healthcare providers and pharmacies handling these syringes are most at risk due to potential contamination.
Check for NDC number 72196-6009-1 on the syringe label. The affected lots range from 36-239063 to 36-255636 with specific expiration dates listed in the recall notice.
Look for the NDC number 72196-6009-1 on the syringe label to confirm if it's affected.
The recall is due to a lack of assurance of sterility, meaning the syringes may not be sterile and could cause infections if used for medical purposes.
Check for the NDC number 72196-6009-1 on the syringe label. The affected lots range from 36-239063 to 36-255636 with specific expiration dates listed in the recall notice.
The recall notice does not specify a remedy, so contact your healthcare provider or pharmacy for guidance on safe disposal or alternatives.
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-0965-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0965-2023 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.
