Medical Device Recalls
-
1 to 10 of 14 Results
510(K) Number: K160176 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Tri-Staple 2.0 Black Intelligent Reload, Product Number SIG60AXT | 2 | 03/06/2023 | Covidien, LP |
EGIA 60 ARTICULATING MED THICK SULU , EGIA60AMT | 2 | 06/16/2019 | Covidien LLC |
EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT | 2 | 06/16/2019 | Covidien LLC |
EGIA 45 ARTICULATING MED THICK SULU, Item Code EGIA45AMT | 2 | 06/16/2019 | Covidien LLC |
EGIA 45 ARTICULATING XTRA THICK SULU, Item Code EGIA45AXT | 2 | 06/16/2019 | Covidien LLC |
EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT | 2 | 06/16/2019 | Covidien LLC |
SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC , SIG60CTAMT | 2 | 06/16/2019 | Covidien LLC |
EGIA 60 CURVED TIP ART MED THICK SULU, EGIA60CTAMT | 2 | 06/16/2019 | Covidien LLC |
EGIA45 CT AR MD THK REL, EGIA45CTAMT | 2 | 06/16/2019 | Covidien LLC |
SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD , SIG30AMT | 2 | 06/16/2019 | Covidien LLC |
-