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Jan 16 (Reuters) - ResMed said its respiratory masks containing magnets will remain on the market even though the U.S. Food and Drug Administration classified a recall of the product as most serious as their use could cause major injuries or death.
The California-based medical device maker, which started the recall process on Nov. 20, said the classification was due to a correction in the labeling and is not a product removal.
The FDA defines a recall as a method of removing or correcting prod...
>>> Read more: ResMed says its masks to remain on market despite FDA classification
The California-based medical device maker, which started the recall process on Nov. 20, said the classification was due to a correction in the labeling and is not a product removal.
The FDA defines a recall as a method of removing or correcting prod...
>>> Read more: ResMed says its masks to remain on market despite FDA classification
