Home › WESTMED, INC. › Adult Elongated Non-Rebreather Mask w/o Safety Valve
Adult Elongated Non-Rebreather Mask w/o Safety Valve
WESTMED, INC. · Model 3108-E · UDI-DI 00709078002861
KGB
Prescription
10
510(k) clearances
165
Adverse events (6 deaths)
8
Recalls
152
Facilities
Description
Adult Elongated Non-Rebreather Mask w/o Safety Valve, 7'Tube
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2020-11-11 | Westmed, Inc. | There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection |
| 2004-07-12 | Medex Inc | The non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex. |
| 2004-07-12 | Medex Inc | The non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex. |
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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.
