fda medwatch1 min read
saveMedical Action Industries issues correction for convenience kits with recalled Namic manifolds
read at fda medwatch ↗CRLNegative
Medical Action Industries has issued a correction notice for certain convenience kits that contain Namic manifolds previously recalled by Medline.
The company advises customers to immediately check inventory, quarantine the kits, remove and destroy the affected manifolds, and apply over‑labels stating the manifolds must not be used.
The FDA classifies this as a Class I recall, the most serious type, because continued use could cause serious injury or death if particulates enter the bloodstream.
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This writeup was produced by pharmadog from original reporting by fda medwatch.
Original headline: “Convenience Kit Correction: Medical Action Industries Issues Correction for Kits Containing Recalled Namic Manifolds”
read at fda medwatch ↗589 words · retrieved 4h ago
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