Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K182354 |
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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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| Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP ... | 2 | 04/28/2020 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 i... | 2 | 01/28/2020 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil... | 2 | 01/28/2020 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
| Telescopic Smoke Evac Pencil, PB, Coated, Product No. SHKTSPCL. The product is a Bovie pencil that ... | 2 | 01/28/2020 |
FEI # 1811755 Stryker Instruments Div. of Stryker Corporation |
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