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U.S. Department of Health and Human Services

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

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ManufacturerBrand NameDate Report Received
ACUMED LLC ARH SOLUTIONS HEAD 22MM, RIGHT 07/25/2020
ZIMMER BIOMET, INC. UNKNOWN NEXEL ARTICULATION KIT 07/01/2020
ZIMMER BIOMET, INC. UNKNOWN NEXEL HUMERAL COMPONENT 07/01/2020
ZIMMER BIOMET, INC. UNKNOWN COONRAD-MOREY ELBOW- HUMERAL COM 06/08/2020
ZIMMER BIOMET, INC. UNKNOWN COONRAD- MOREY ULNA COMPONENT 06/08/2020
ZIMMER BIOMET, INC. UNKNOWN COONRAD-MOREY ELBOW HUMERAL COMP 06/08/2020
ZIMMER BIOMET, INC. UNK HUMERAL 06/04/2020
ZIMMER BIOMET, INC. UNK HUMERAL 06/04/2020
ZIMMER BIOMET, INC. UNKNOWN HUMERAL 06/02/2020
ZIMMER BIOMET, INC. UNK C-M ULNAR COMPONENT 06/01/2020
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