Medical Device Recalls
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1 to 10 of 18 Results
510(K) Number: K071923 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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FLIXENE, 6X50, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. | 2 | 06/04/2024 | Atrium Medical Corporation |
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