Central Admixture Pharmacy Services recalls hydro morphine syringes with lot numbers 17-275680, 17-275945, and 17-276094 due to lack of sterility assurance. These syringes are for prescription use only in central pharmacy settings.
Lack of assurance of sterility:
Central Admixture Pharmacy Services has recalled specific hydro morphine syringes because they may not be sterile. This could lead to infections if used improperly. The affected products are for prescription use only in central pharmacy settings.
The syringes lack assurance of sterility, meaning they might not be clean enough to prevent infections. This is a risk in medical settings where sterile injections are critical. However, the recall is for specific lot numbers and not all hydro morphine syringes.
Healthcare professionals and patients receiving hydro morphine injections through central pharmacy services. Those using the recalled syringes for prescription purposes are most at risk.
Check the lot number on the syringe label: 17-275680, 17-275945, or 17-276094. These syringes are for prescription use only in central pharmacy settings and have specific expiration dates.
Look for lot numbers 17-275680, 17-275945, or 17-276094 on the syringe label.
The recall indicates a lack of sterility assurance, so these syringes should not be used until replaced with a safe product.
Check the lot number on the syringe label. If it matches 17-275680, 17-275945, or 17-276094, stop using it and contact your pharmacy for a replacement.
The recalled syringes are for prescription use only in central pharmacy settings and have specific lot numbers: 17-275680, 17-275945, or 17-276094.
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-0027-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0027-2024 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.
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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.
