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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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83 records meeting your search criteria returned- Product Code: LWF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
WEBTEC DIV OF SCARPA HEALTHCARE BREATHE RIGHT NASAL STRIPS EXTRA 12/17/2018
WEBTEC DIV OF SCARPA HEALTHCARE BREATHE RIGHT NASAL STRIPS 12/17/2018
EQUATE / PERRIGO COMPANY EQUATE NASAL STRIPS 06/27/2018
WEBTEC DIV OF SCARPA HEALTHCARE BREATHE RIGHT NASAL STRIPS EXTRA 04/24/2018
ASO LLC EQUATE 03/29/2018
ASO LLC CVS HEALTH 03/15/2018
ASO LLC KROGER 03/01/2018
ASO LLC KROGER 02/14/2018
ASO LLC MEMBER'S MARK 12/01/2017
ASO LLC CVS HEALTH 09/26/2017
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