SleepmateSnoring Piezo Sensor
Ambu A/S · Model 812200-000 · UDI-DI 05707480042425
BZQ
Prescription
10
510(k) clearances
127
Adverse events (11 deaths)
3
Recalls
110
Facilities
Description
Snoring Piezo Sensor (Sleepmate item 1250)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-21 | Salter Laboratories, Division of Regulatory Affairs | The incorrect length and connector were utilized in lot 110810 of the ThermiSense Alice 5, making the product unusable as it will not interface with the sleep labs equipment. |
| 2004-06-04 | Respironics, Inc. | Recalling firm received a product complaint from a customer that the lead wire from Model 915 battery was not connected. |
| 2004-05-24 | CAS Medical Systems, Inc. | Device may not alarm for %SpO2 value limit violations if a specific feature is enabled |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.