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SonarMed Inc. Recalls Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty
SonarMed Inc. is recalling SonarMed Airway acoustic sensors due to a restricted inner diameter of SonarMed Airway resulting in difficulty passing a suction catheter through the sensor (2.5mm, 3.0mm, and 3.5mm).
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
Questions?
If you have questions about this recall, contact Medtronic Representative or Customer Service at 800-962-9888, Option 2.
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