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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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111 records meeting your search criteria returned- Product Code: PAO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ARCOM XL STANDARD HUMERAL BEARING 12/13/2017
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE HUMERAL TRAY 12/13/2017
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE HUMERAL TI TRAY 44 11/20/2017
ZIMMER BIOMET, INC. UNKNOWN BEARING 11/02/2017
ZIMMER BIOMET, INC. UNKNOWN E1 STANDARD HUMERAL BEARING 11/02/2017
ZIMMER BIOMET, INC. COMP RVRS SHLDR GLNSP STD 36MM 09/28/2017
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE SHOULDER GLENOSPHE 05/18/2015
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE 3.5MM HEX DRIVER 05/14/2015
BIOMET ORTHOPEDICS UNKNOWN SHOULDER 12/15/2014
BIOMET ORTHOPEDICS ARCOM XL 44-36 RTNV+3 HMRL BRG 12/11/2014
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