Medical Device Recalls
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91 to 100 of 500 Results
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Recall Date to: 04%2F08%2F2014 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Mojo 2 Full Face AAV Non Vented Mask, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| iQ 2 Nasal Vented Mask | 1 | 04/01/2024 | SleepNet Corporation |
| Phantom 2 Nasal Vented Mask | 1 | 04/01/2024 | SleepNet Corporation |
| Mojo 2 Full Face Non Vented Mask, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| Mojo Non Vented Full Face Mask with Headgear, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| Mojo Full Face with Headgear, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| Mojo 2 Full Face Vented Mask, All Sizes | 1 | 04/01/2024 | SleepNet Corporation |
| GeoMed Custom Tracecarts, REF Numbers: a) 53-1831 ORTHO TOTAL JOINT TRACECART, b) 53-1836 GENERAL S... | 1 | 03/29/2024 | DeRoyal Industries Inc |
| Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT107... | 1 | 03/28/2024 | InfuTronix LLC |
| Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); ... | 1 | 03/28/2024 | InfuTronix LLC |
| * The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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