Central Admixture Pharmacy Services recalls specific lots of succinylcholine 200 mg/10 mL syringes because validation data for decontamination cycles is lacking, posing a risk of contamination.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled certain lots of succinylcholine 200 mg/10 mL syringes (Rx only) due to a lack of assurance of sterility. This could lead to contamination if the product is used in medical procedures.
The product was repackaged by CAPS Inc without sufficient validation data for decontamination cycles. This means the syringes may not be sterile, which could cause infections or other complications during medical procedures.
Healthcare professionals and patients who have received the recalled succinylcholine syringes for medical use are at risk. The most vulnerable are those using the product in critical care settings.
Check for the product name 'succinylcholine 200 mg/10 mL (20 mg/mL), Syringe, Rx only'. The lots listed in the recall (e.g., 36-238812, 36-238813, etc.) and expiration dates (e.g., 7/10/2023) indicate the affected items.
Identify the lot numbers and expiration dates listed in the recall notice to determine if your syringes are affected.
The product was repackaged by CAPS Inc without sufficient validation data for decontamination cycles, which could lead to contamination.
The recall notice does not specify a remedy, so contact your healthcare provider for guidance on safe alternatives.
Yes, the recall includes specific lot numbers such as 36-238812, 36-238813, and others listed in the notice with corresponding expiration dates.
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-0949-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0949-2023 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.
