Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K833586 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design M Malar Sizer Set (Silicone, No... | 2 | 02/08/2017 |
FEI # 3002821504 Stryker Leibinger GmbH & Co. KG |
| QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Cent... | 2 | 02/08/2017 |
FEI # 3002821504 Stryker Leibinger GmbH & Co. KG |
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