(AOF) – Following the publication of our latest dispatch on ResMed, the company wished to provide several clarifications. It indicates that its brand’s magnet masks “are not the subject of a recall but more simply of an update of the instructions concerning interference, when the magnet masks are near implanted medical devices ( e.g. pacemakers, implantable cardioverter defibrillators (ICDs), neurostimulators, cerebrospinal fluid (CSF) shunts, insulin or infusion pumps).”
She adds that the term “recall” used by the FDA represents different situations, including product recall. “However, the notion of recall in French can easily lead to confusion, because it is very often understood as implying a withdrawal of products. In this case, it is an update of contraindications and warnings of these masks with magnets”, emphasizes ResMed.
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