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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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95 records meeting your search criteria returned- Product Code: ITQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DJO, LLC FULLFORCE,ACL,SHRT CF,RT,L 02/27/2019
DJO, LLC DEFIANCE FP 02/27/2019
DJO, LLC TITANIUM, A22 01/30/2019
DJO, LLC DEFIANCE FP PLUS 01/25/2019
DJO, LLC DONJOY TITANIUM, A22 01/17/2019
DJO, LLC DONJOY 06/05/2018
DJO, LLC DONJOY 05/07/2018
DJO, LLC DONJOY 05/07/2018
DJO, LLC DONJOY 04/27/2018
DJO, LLC DONJOY 02/28/2018
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