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Old 04-29-2024, 01:10 PM #1
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MuonOne MuonOne is offline
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MuonOne MuonOne is offline
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Help SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of A

SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty
SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty | FDA
SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty | FDA

The FDA regards this as a "Class I recall," the most serious variety.
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