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HomeDevice types › DPT

Probe, Blood-Flow, Extravascular

FDA product code DPT · Class 2 · Cardiovascular

209
Registered devices
398
Adverse events
24
Recalls
48
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d
2024-09-24Smiths Medical ASD, Inc.Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device d

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.