Edge Pharma recalls single-use IV syringes due to lack of sterility assurance. Affected products were sold between December 2021 and February 2022. Consumers should contact the company for details.
Lack of Assurance of Sterility
Edge Pharma is recalling single-use IV syringes that may not be sterile. This could lead to infections if used for injections. The recall covers specific syringes sold between December 2021 and February 2022.
The syringes lack assurance of sterility, meaning they might not be clean enough to prevent infections. If used for injections, this could lead to serious infections in the body.
Healthcare professionals and patients using the recalled IV syringes for injections. Those who have used the syringes for medical procedures are most at risk.
Check for the product name 'Phenylephrine HCl, 1mg/10mL (0.1mg/mL), 10 mL per syringe, Single Use Syringe for IV Injection' from Edge Pharma. The recall covers syringes sold between December 2021 and February 2022.
Look for the product name and NDC code 05446-1544-10 on the syringe label.
The syringes lack assurance of sterility, which could lead to infections if used for injections.
The syringes were sold between December 2021 and February 2022.
The recall record does not specify a remedy or replacement process.
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0416-2022 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0416-2022 from Edge Pharma. 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.
