Central Admixture Pharmacy Services recalls specific lots of diphenhydramine 50mg in 0.9% sodium chloride solution after FDA found potential sterility issues. This affects pharmacy-prepared medications for medical use.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling certain lots of diphenhydramine 50mg added to 0.9% sodium chloride solution. The recall follows an FDA inspection that raised concerns about the sterility of these products, which are intended for medical use only.
The FDA inspection found potential issues with the sterility of the medication. This means the product could be contaminated with bacteria, which could cause serious infections if used improperly.
Pharmacies and healthcare facilities that prepared the recalled medication using the specific lots listed. Patients receiving this medication through their healthcare providers are at risk if they were given the recalled product.
Check the lot numbers: 37-884155 through 37-892475. These products were manufactured for pharmacy use and expire by May 2023 or later. They are labeled as diphenhydramine 50mg added to 0.9% sodium chloride solution.
Look for the lot numbers listed in the recall: 37-884155 through 37-892475.
The FDA inspection raised concerns about sterility, so the medication is not safe for use. Healthcare providers should stop using these specific lots.
If you have the recalled medication, contact your pharmacy to stop using it and get a replacement.
Check the lot numbers on the product: 37-884155 through 37-892475. These are specific pharmacy-prepared medications for medical use.
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-0738-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0738-2023 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.
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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.
