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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 OA NANO, MEDIAL, RT, S 06/26/2019
DJO, LLC DONJOY FULLFORCE,ACL,STD,CALF,LT,M 06/26/2019
DJO, LLC DONJOY ARMOR FP,ACL,LT,M 06/26/2019
DJO, LLC DONJOY ARMOR,ACL,STD,RT,M 06/26/2019
DJO, LLC DONJOY FULLFORCE,ACL,SHRT CF,LT,XS 06/26/2019
DJO, LLC DONJOY ARMOR FP, ACL,STD,RT,M 06/26/2019
DJO, LLC DONJOY FULLFORCE,ACL,SHRT CF,RT,M 06/26/2019
DJO, LLC DONJOY ARMOR FP,ACL,RT,S 06/26/2019
DJO, LLC DONJOY COOL, X-ACT ROM, POST-OP 06/26/2019
DJO, LLC DONJOY FULLFORCE,ACL,STD,CALF,LT,M 06/26/2019
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