SonarMed AirWave Monitor, Model Number M0001
Reported: September 11, 2019 Initiated: April 17, 2017 #Z-2450-2019
Product Description
SonarMed AirWave Monitor, Model Number M0001
Reason for Recall
Potential for the presence of two error codes which would make the monitor inoperable.
Details
- Recalling Firm
- SonarMed Inc
- Units Affected
- 16 units
- Distribution
- CA & TX
- Location
- Carmel, IN
Frequently Asked Questions
What product was recalled? ▼
SonarMed AirWave Monitor, Model Number M0001. Recalled by SonarMed Inc. Units affected: 16 units.
Why was this product recalled? ▼
Potential for the presence of two error codes which would make the monitor inoperable.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 11, 2019. Severity: Moderate. Recall number: Z-2450-2019.
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