Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032406 |
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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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This product is a single use sterile device that is used to direct the lesion to the targeted site. ... | 2 | 07/03/2024 | Stryker Corporation |
RF Cannula, 100 mm,Curved 5 MM, 20 G, REF 0406-630-115 RX only, Disposable ( 10/pk) Product Us... | 2 | 08/02/2012 | Stryker Instruments Div. of Stryker Corporation |
RF Cannula, 100 mm,Curved 10 MM, 20 G, REF 0406-630-125 RX only, Disposable ( 10/pk) Product U... | 2 | 08/02/2012 | Stryker Instruments Div. of Stryker Corporation |
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