Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K050503 |
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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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NA-201SX-4022-ASPIRATION NEEDLE VIZISHOT 22G, model no. NA-201SX-4022-A - Product Usage: Used with u... | 2 | 02/05/2021 | Aomori Olympus Co., Ltd. |
NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G, model no. NA-201SX-4021 - Product Usage: Used with ult... | 2 | 02/05/2021 | Aomori Olympus Co., Ltd. |
NA-201SX-4022-C ASPIRATION NEEDLE ViziShot 22G w/o stylet, model no. NA-201SX-4022-C - Product Usage... | 2 | 02/05/2021 | Aomori Olympus Co., Ltd. |
NA-201SX-4022-B ASPIRATION NEEDLE ViziShot 22G, model no. NA-201SX-4022-B - Product Usage: Used with... | 2 | 02/05/2021 | Aomori Olympus Co., Ltd. |
OLYMPUS ViziShot EBUS Aspiration Needle Endobronchial Ultrasound (EBUS) Needle for Fine Needle As... | 2 | 10/07/2011 | Olympus America Inc. |
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