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The FDA said ResMed was recalling these masks to update the labels and add more warnings and information. The California-based medical device maker started the recall process on Nov. 20 and has ...
The FDA defines a recall as a method of removing or correcting products that are in violation of laws administered by the health regulator and does not include a market withdrawal. ResMed's masks ...
ResMed Inc. is an American medical equipment company based in San Diego, California.It primarily provides cloud-connectable medical devices for the treatment of sleep apnea (such as CPAP devices and masks), chronic obstructive pulmonary disease (COPD), and other respiratory conditions.
The application of positive pressure may be intended to prevent upper airway collapse, as occurs in obstructive sleep apnea, or to reduce the work of breathing in conditions such as acute decompensated heart failure. CPAP therapy is highly effective for managing obstructive sleep apnea.
USA: February 1, 2023; Conagra Brands issued a major recall of nearly 2.6 million pounds of canned meat and poultry due to a packaging defect that may cause the food to get contaminated. [142] USA: February 9, 2023; Colgate-Palmolive issued a recall of nearly 5 million bottles of Fabuloso multi-purpose cleaner due to a risk of bacterial growth ...
Within SaaS, ResMed (RMD) shows strong momentum in the Brightree service portfolio.
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The protection provided by an FFP2 (or FFP3) mask includes the protection provided by a mask of the lower-numbered classes. A mask conforming to the standard must have its class written on it, along with the name of the standard and its year of publication, as well as any applicable option codes, e.g. “EN 149:2001 FFP1 NR D”.
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