Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K944210 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Endoscopy FloControl Arthroscopy Pump Integrated Tubing, Model number 0350600006, for use wi... | 2 | 01/21/2009 | Stryker Endoscopy |
| Inflow/Outflow Cannula; Qty: 1; distributed by Stryker Endoscopy, 5900 Optical Court, San Jose, CA... | 2 | 04/08/2011 | Stryker Endoscopy |
| Dri-Lok Disposable Cannula, Part numbers 3910-075-500, 3910-075-501, 3910-075-502, 3910-075-650, 391... | 2 | 01/16/2009 | Stryker Endoscopy |
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