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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 13 Results
510(K) Number: K940230
 
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Product Description
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FDA Recall
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Endotrig ETF Hook Blade, Catalog Number 1052-1 The EPF system is designed for the treatment of pl... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac EPF/EGR Triangle Blade, Catalog Number 3054-1 The EPF system is designed for the treatm... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system is designed for t... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment ... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac EPF/EGR Hook Blade, Catalog Number 3055-1 The EPF system is designed for the treatment ... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the t... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the ... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of ... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of ... 2 08/28/2019 FEI # 3002807830
Stryker GmbH
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