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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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75 records meeting your search criteria returned- Product Code: GDW Product Problem: Device Packaging Compromised Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, LLC. ECHELON FLEX 09/16/2016
ETHICON ENDO-SURGERY, LLC. ECHELON FLEX ENDOCUTTER 07/19/2016
ETHICON ENDO-SURGERY, LLC. ECHELON RELOAD 07/05/2016
ETHICON ENDO-SURGERY, LLC. POWERED ECHELON PLUS 07/05/2016
ETHICON ENDO-SURGERY, LLC. STAPLE, IMPLANTABLE 06/29/2016
ETHICON ENDO-SURGERY, LLC. ECHELON FLEX ENDOCUTTER 06/29/2016
ETHICON ENDO-SURGERY, LLC. PROXIMATE LINEAR STAPLER 05/27/2016
ETHICON ENDO-SURGERY, LLC. STAPLE, IMPLANTABLE 05/03/2016
ETHICON ENDO-SURGERY, LLC. CONTOUR CURVED CUTTER STAPLER RELOAD 04/20/2016
ETHICON ENDO-SURGERY, LLC. STAPLE, IMPLANTABLE 04/08/2016
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