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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 DEFIANCE III FP 04/15/2020
DJO LLC. DONJOY TITANIUM, A22 04/14/2020
DJO, LLC DONJOY DEFIANCE FP 03/23/2020
DJO, LLC DONJOY DEFIANCE III FP 03/09/2020
DJO, LLC DONJOY DEFIANCE FP 02/27/2020
DJO, LLC DONJOY FULLFORCE,ACL,SHRT CF,RT,XS 02/14/2020
DJO, LLC DONJOY DEFIANCE III 02/11/2020
DJO, LLC DONJOY FULLFORCE,ACL,SHRT CF,LT,M 02/03/2020
DJO, LLC DONJOY ARMOR FP, ACL,STD,RT,XL 01/13/2020
DJO, LLC DONJOY FULLFORCE,ACL,STD,CALF,RT,S 01/13/2020
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