Home › SLEEPNET, CORP. › Innova Nasal Non Vented Mask, s/m
Innova Nasal Non Vented Mask, s/m
SLEEPNET, CORP. · Model 50592 · UDI-DI 00814747021897
BYG
Prescription
10
510(k) clearances
542
Adverse events (9 deaths)
41
Recalls
269
Facilities
Description
Nasal non vented mask for use with non invasive ventilator system with exhalation valve.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-21 | Medline Industries, LP | Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortnes |
| 2018-07-11 | POM Medical LLC | Complaints were received on the product, such as the re-breather bag would not fill/inflate or the oxygen line pops off after the oxygen is turned on due to a clogged port. |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc | Reports of tubing detaching from oxygen masks either prior to use (in packaging) or during use were made by different end users and for different batches. The failures were caused |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc | |
| 2017-05-10 | ConvaTec, Inc |
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.
