Central Admixture Pharmacy Services recalls tromethamine 0.3 Molar 50mL syringes (NDC 71285-8086-2) due to potential sterility issues found during FDA inspection. Affected lots expire May 2023.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling tromethamine 0.3 Molar 50mL syringes that may not be sterile. This is serious because medical-grade syringes must be sterile for safe use in patient treatments.
FDA inspections found these syringes may not be sterile. Medical syringes intended for patient use must be sterile to prevent infections. Using non-sterile syringes could cause serious infections in patients.
Healthcare professionals using these syringes for patient medication preparation. Patients receiving treatments with these syringes are at risk of infection.
Check for lot numbers 37-884580, 37-887061, or 37-892981 with expiration dates May 2023 or earlier. These syringes are for prescription-only use by healthcare providers.
Immediately discard any syringes with lot numbers 37-884580, 37-887061, or 37-892981 that expire by May 2023.
FDA inspections found these syringes may not be sterile, which could lead to infections in patients.
Immediately discard syringes with lot numbers 37-884580, 37-887061, or 37-892981 that expire by May 2023.
No, these syringes may not be sterile and could cause infections if used for patient treatments.
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-0741-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0741-2023 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.
