Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2016-09-23 | VAI | Voluntary action indicated | SureTek Medical | 1 |
| 2016-09-23 | VAI | Voluntary action indicated | SureTek Medical | 1 |
| 2016-03-03 | WL | Warning Letter | SureTek Medical | — |
| 2016-03-03 | WL | Warning Letter | SureTek Medical | — |
| 2015-11-10 | OAI | Official action indicated | SureTek Medical | 8 |
| 2015-11-10 | OAI | Official action indicated | SureTek Medical | 8 |
| 2012-07-25 | VAI | Voluntary action indicated | SureTek Medical | 6 |
| 2012-07-25 | VAI | Voluntary action indicated | SureTek Medical | 6 |
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