Central Admixture Pharmacy Services recalls specific hydrocodone syringes (NDC 71286-2012-1) due to lack of sterility assurance. Affected units have lot numbers ending in 17-275339 through 17-276027 with expiration dates through October 2023.
Lack of assurance of sterility:
Central Admixture Pharmacy Services has recalled certain hydrocodone syringes because they may not be sterile. This could lead to infections if used improperly. The affected products were manufactured for hospital use and have specific lot numbers and expiration dates.
The syringes may not be sterile, which could lead to infections if used for injections. This is a risk for healthcare settings where the syringes are used for intravenous medication administration. The lack of sterility assurance means the product could introduce harmful bacteria into the patient's body.
Healthcare facilities and medical professionals who use these syringes for intravenous administration. Patients receiving treatment with these specific syringes are at risk if the product is not sterile.
Check for the NDC number 71286-2012-1 on the syringe label. Look for lot numbers starting with 17-275339 through 17-276027 with expiration dates through October 2023.
Look for the NDC number 71286-2012-1 and lot numbers starting with 17-275339 through 17-276027.
Hydrocodone syringes with NDC 71286-2012-1, lot numbers 17-275339 through 17-276027, and expiration dates through October 2023.
The product may not be sterile, which could lead to infections if used for intravenous administration.
Check the syringe label for the NDC number 71286-2012-1 and lot numbers starting with 17-275339 through 17-276027.
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-0031-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0031-2024 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.
