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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K040369
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Product Description
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Recall
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FDA Recall
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IBO Blade, Right, for use with Stryker TPS Reciprocating Saw, REF 5100-37-901, Stryker Instruments, ... 2 11/16/2011 Stryker Instruments Div. of Stryker Corporation
Right IBO Blade , for use with Stryker TPS Reciprocating Saw, REF 5100-37-901S2, Stryker Instruments... 2 11/16/2011 Stryker Instruments Div. of Stryker Corporation
Right/Left IBO Blade Set, for use with Stryker TPS Reciprocating Saw, REF 5100-37-903, Stryker Instr... 2 11/16/2011 Stryker Instruments Div. of Stryker Corporation
Left IBO Blade , for use with Stryker TPS or Core Reciprocating Saw, REF 5100-37-902S2, Stryker Inst... 2 11/16/2011 Stryker Instruments Div. of Stryker Corporation
IBO Blade, Left, for use with Stryker TPS Reciprocating Saw, REF 5100-37-902, Stryker Instruments, K... 2 11/16/2011 Stryker Instruments Div. of Stryker Corporation
Stryker Instruments 2.1 mm Cross-Cut Fissure Bur, carbide extended, sterile; REF 2296-101-621. 2 11/16/2009 Stryker Instruments Div. of Stryker Corporation
Stryker brand Consolidated Operating Room Equipment (CORE) SystemPowered Instrument Driver, REF 5400... 2 08/23/2005 Stryker Instruments Div. of Stryker Corporation
Stryker brand Consolidated Operating Room Equipment (CORE) System Powered Instrument Driver, REF 540... 2 08/23/2005 Stryker Instruments Div. of Stryker Corporation
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