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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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181 records meeting your search criteria returned- Product Code: PBI Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. G7 NEUTRAL ARCOMXL LNR 32MM G 06/18/2019
ZIMMER BIOMET, INC. G7 HI-WALL E1 LINER 06/18/2019
ZIMMER BIOMET, INC. G7 PPS LTD ACET SHELL 50D 06/11/2019
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 32MM D 06/11/2019
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 36MM F 05/31/2019
ZIMMER BIOMET, INC. G7 PPS LTD ACET SHELL 54F 05/14/2019
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 36MM F 04/24/2019
. G7 PPS LTD ACET SHELL 54F 04/24/2019
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 36MM D 04/22/2019
ZIMMER BIOMET, INC. G7 HI-WALL ARCOMXL LNR 36MM G 03/29/2019
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