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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
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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: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. G7 HI-WALL E1 LINER 32MM B 07/25/2023
ZIMMER BIOMET, INC. G7 PPS LTD ACET SHELL 46B 07/25/2023
ZIMMER BIOMET, INC. G7 FREEDOM CONST E1 LNR 36MM G 06/23/2023
ZIMMER BIOMET, INC. G7 PPS LTD ACET SHELL 58G 06/21/2023
ZIMMER BIOMET, INC. G7 HI-WALL E1 LINER 36MM G 06/21/2023
ZIMMER BIOMET, INC. G7 HI-WALL ARCOMXL LNR 36MM D 06/20/2023
ZIMMER BIOMET, INC. G7 NEUTRAL ARCOMXL LNR 36MM G 06/01/2023
ZIMMER BIOMET, INC. G7 PPS LTD ACET SHELL 52E 05/26/2023
ZIMMER BIOMET, INC. G7 NEUTRAL E1 LINER 36MM G 05/23/2023
ZIMMER BIOMET, INC. G7 FREEDOM CONST E1 LNR 36MM G 05/22/2023
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