Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K143077 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Trevo(TM) XP ProVue Procedure Pack, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm, .Excelsior(TM) XT-27... | 2 | 12/05/2017 | Stryker Neurovascular |
| Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm; Excelsior(TM) XT-27(... | 2 | 12/05/2017 | Stryker Neurovascular |
| Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, ... | 2 | 12/05/2017 | Stryker Neurovascular |
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