Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K121796 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 10mm Weck® Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories... | 2 | 03/25/2014 |
FEI # 3005747797 Teleflex Medical |
| 12mm Weck® Vista" Cannula-only, Teleflex Medical, Product Usage: An endoscope and accessories... | 2 | 03/25/2014 |
FEI # 3005747797 Teleflex Medical |
| 10mm Weck Vista Cannula-only, Catalog No. 405910C, 12mm Weck Vista Cannula-only, Catalog No. 405912C... | 2 | 04/02/2014 |
FEI # 3005747797 Teleflex Medical |
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