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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 DONJOY TITANIUM, A22 06/17/2019
DJO, LLC DONJOY DEFIANCE III FP 06/11/2019
DJO, LLC DONJOY TITANIUM, A22 06/03/2019
DJO, LLC DONJOY FULLFORCE,ACL,SHRT CF,LT,XL 05/22/2019
DJO, LLC DEFIANCE III FP 04/08/2019
BREG, INC. FUSION OA 04/05/2019
DJO, LLC DEFIANCE FP PLUS 04/03/2019
DJO, LLC DEFIANCE FP 04/03/2019
DJO, LLC DONJOY FULLFORCE,ACL,STD,CALF,RT,XS 03/28/2019
DJO, LLC ARMOR FP,ACL,LT,M 03/15/2019
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