Central Admixture Pharmacy Services recalls neostigmine syringes due to lack of sterility assurance. This drug was repacked by CAPS, Inc. in Phoenix, AZ. Affected lots expire through August 2023.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services recalls neostigmine 5 mg/5mL syringes that were repacked by CAPS, Inc. in Phoenix. The recall is due to a lack of assurance of sterility, which could lead to infections if used.
The syringes were repacked by CAPS, Inc. without sufficient validation data for decontamination cycles. This lack of sterility assurance means the product could be contaminated, potentially causing infections if used.
Prescription drug users who received neostigmine syringes repacked by CAPS, Inc. in Phoenix, AZ. Healthcare professionals and patients using these syringes for medical treatment are at risk.
Check for the NDC code 72196-6065-1 and lot numbers 36-239285, 36-239287, 36-239456, 36-239873, 36-240994-36-240997, 36-241447, 36-242407-36-242408, 36-246298, 36-248998, 36-251613, or 36-251781. These syringes expire through August 2023.
Identify the NDC code and lot numbers listed in the recall notice to confirm if your syringe is affected.
The recall is due to a lack of assurance of sterility. Validation data for decontamination cycles is lacking, which could lead to contamination.
The recall notice does not specify a remedy, so contact your healthcare provider or the manufacturer for guidance.
Check for the NDC code 72196-6065-1 and lot numbers listed in the recall notice, which expire through 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-0982-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0982-2023 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.
