Central Admixture Pharmacy Services recalls morphine syringes due to lack of sterility assurance from sanitization cycles. Affected lots expire by July 2023. No remedy specified in official notice.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling morphine syringes that may not be sterile due to insufficient sanitization validation. This could lead to infections if used improperly. The recall affects specific lots with expiration dates through July 2023.
The syringes lack validated sanitization cycles, meaning they might not be sterile when used. This could cause infections if the medication is injected improperly. The risk is specific to medical use where sterility is critical.
Prescription patients using the recalled morphine syringes for pain management. Healthcare providers preparing these medications in pharmacies are at higher risk due to the sterile nature of the product.
Check for the lot numbers 17-271060 through 17-272785 with expiration dates up to August 2023. The product is a prescription-only morphine syringe in 0.9% sodium chloride solution.
Identify the lot number and expiration date on the syringe label to confirm if it's affected.
The official recall notice states the syringes lack validated sanitization cycles, so they may not be sterile. Do not use until confirmed safe.
The recall notice does not specify a remedy, so contact the manufacturer directly for guidance.
Look for lot numbers 17-271060 through 17-272785 with expiration dates up to August 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-1068-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1068-2023 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.
