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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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103 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. UNKNOWN REVERSE SCREW 02/04/2020
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE GLENOSPHERE 36MM + 08/31/2018
ENCORE MEDICAL L.P. ALTIVATE SHOULDER 07/27/2018
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE E1 44-36 STANDARD 05/24/2018
ENCORE MEDICAL L.P. ALTIVATE SHOULDER 05/03/2018
ZIMMER BIOMET, INC. ARCOM XL 44-36 STD HMRL BRNG 01/15/2018
ZIMMER BIOMET, INC. COMP RVSR SHLDR GLNSP +3 36MM 01/15/2018
ZIMMER BIOMET, INC. COMPREHENSIVE NON-LOCKING SCREW 12/13/2017
ZIMMER BIOMET, INC. COMP LOCKING SCREW 4.75X20MM 12/13/2017
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE SHOULDER CENTRAL S 12/13/2017
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