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FDA Announces Voluntary Nationwide Recall of Edge Pharma Drug Products

The FDA recently announced that all drugs manufactured by Edge Pharma, LLC are being voluntarily recalled due to process issues that could lead to problems with products intended to be sterile.  The products pose a risk of life-threatening infections.  For a link to lot numbers, distribution dates and drug information click here: https://edgepharma.com/assets/recalledproducts.pdf

The drug products manufactured by Edge Pharma include many medications as well products such as IV bags, syringes, vials, bottles and jars.  These products were distributed nationwide and directly to customers and medical facilities.  The products can be identified by the label containing the Edge Pharma, LLC name and logo.

For questions regarding this recall, consumers can contact Edge Pharma by phone (802-992-1178) or e-mail: Recall@edgepharma.com, Monday through Friday from 8:00 am to 4:00 pm, EST.

For access to this FDA announcement and a list of the medications recalled, click here:

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/edge-pharma-llc-issues-voluntary-nationwide-recall-all-drug-products-due-lack-sterility-assurance

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