Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K940967 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Endoscopic Curved Intraluminal Stapler, 21 mm diameter, Model ECS21A The Ethicon Endo-Surgery Int... | 1 | 05/15/2019 | Ethicon Endo-Surgery Inc |
Endoscopic Curved Intraluminal Stapler, 33 mm diameter, Model ECS33A The Ethicon Endo-Surgery Int... | 1 | 05/15/2019 | Ethicon Endo-Surgery Inc |
Endoscopic Curved Intraluminal Stapler, 29 mm diameter, Model ECS29A The Ethicon Endo-Surgery Int... | 1 | 05/15/2019 | Ethicon Endo-Surgery Inc |
Endoscopic Curved Intraluminal Stapler, 25 mm diameter, Model ECS25A The Ethicon Endo-Surgery Int... | 1 | 05/15/2019 | Ethicon Endo-Surgery Inc |
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