Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K081510 |
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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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Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical... | 2 | 03/30/2020 | Trilliant Surgical, LLC |
Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE; Combined Tiger/Headless Screw Part # 210-... | 2 | 08/26/2015 | Trilliant Surgical Ltd. |
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated... | 2 | 08/24/2015 | Trilliant Surgical Ltd. |
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Coun... | 2 | 08/19/2015 | Trilliant Surgical Ltd. |
2.0/2.4 Cannulated Screw Driver Bit, part #210-24-003 | 2 | 04/26/2010 | Trilliant Surgical LTD |
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