FDAAugust 16, 2019device
Irrisept Wound Debridement and Cleansing System. 12 units per case.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Potential defect in the sterile pouch seal, which may result in a lack of sterility assurance.
What to do
FDA enforcement status: Terminated
Brands named
irrimax
Recall history
No related federal recalls on record for this brand yet.
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