Central Admixture Pharmacy Services recalls phenylephrine IV solution (NDC 71285-6092-1) due to particulate matter. Affected lots expire March 2025. Discard immediately if you have these lots.
Presence of Particulate Matter
Central Admixture Pharmacy Services is recalling phenylephrine IV solutions that may contain particulate matter. This could cause serious injury if injected into a patient. The affected products were made in specific lots with expiration dates in March 2025.
Particulate matter in the solution can enter the bloodstream during injection, potentially causing blockages, infections, or severe reactions. This risk is especially dangerous for patients receiving critical medical care.
Healthcare professionals using these IV solutions in medical settings. Patients receiving injections from these products are at risk of serious injury or death.
Check the product label for the lot numbers 37-928390, 37-928796, or 37-928839. These solutions expire by March 2025 and are only available for prescription use in central pharmacy settings.
If you have the recalled phenylephrine IV solutions with the listed lot numbers, discard them safely and do not use.
Lot numbers 37-928390, 37-928796, and 37-928839.
The products expire by March 2025.
No, these specific lots contain particulate matter that can cause serious injury if injected.
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-0272-2025 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0272-2025 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.
