Manual Resuscitator Recall: Ambu Inc. Removes SPUR II Resuscitators Due to Blocked Manometer Port

FDA Recalls · 2025-08-29T04:00:00+0000

A blocked manometer port on the Ambu SPUR II resuscitator may delay ventilation or cause barotraumaView the full article

By FDA Recalls
August 29, 2025 in Recalls

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