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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 17 Results
510(K) Number: K020779
 
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Product Description
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FDA Recall
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Endopath EZ45 Endoscopic Linear Cutter (EZ45B) 2 02/01/2005 Ethicon Endo-Surgery
Endopath EZ45 No Knife Linear Stapler (NK45B). 2 02/01/2005 Ethicon Endo-Surgery
Endopath EZ45 Endoscopic Linear Cutter (EZ45G). 2 02/01/2005 Ethicon Endo-Surgery
Endopath EZ45 Endoscopic Linear Cutter (ET45B). 2 02/01/2005 Ethicon Endo-Surgery
Endopath EZ45 Endoscopic Linear Cutter (ET45G). 2 02/01/2005 Ethicon Endo-Surgery
Endopath EZ45 No Knife Linear Stapler (NK45G). 2 02/01/2005 Ethicon Endo-Surgery
Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter, 35mm Standard, Product... 2 12/17/2003 Ethicon Endo-Surgery
Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter, 35mm Vascular/Thin, Pr... 2 12/17/2003 Ethicon Endo-Surgery
Proximate Linear Cutter with Safety Lock-Out, Reloadable, contains 100 titanium staples with integra... 3 07/08/2003 Ethicon Endo-Surgery
Proximate Linear Cutter with Safety Lock-Out, reloadable, contains 100 titanium staples with integra... 3 07/08/2003 Ethicon Endo-Surgery
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