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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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69 records meeting your search criteria returned- Product Code: OQG Product Problem: Device Contaminated During Manufacture or Shipping Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. TPRLC XR T1 PPS 17X154MM MM T1 02/11/2020
ZIMMER BIOMET, INC. TAPERLOC XR MP T1 PPS 13X111MM 111MM T1 01/10/2020
ZIMMER BIOMET, INC. TPRLC XR T1 PPS 17X154MM 12/26/2019
ZIMMER BIOMET, INC. TPRLC XR T1 PPS 15X150MM 12/26/2019
ZIMMER BIOMET, INC. NEUTRAL LINER 36 MM 12/12/2019
ZIMMER BIOMET, INC. NEUTRAL LINER 36 MM I.D. SIZE II FOR USE 12/04/2019
ZIMMER BIOMET, INC. NEUTRAL LINER 36 MM I.D. SIZE II FOR USE 11/27/2019
ZIMMER BIOMET, INC. TPRLC XR MP FP T1 PPS 5X95MM 03/25/2019
MAKO SURGICAL CORP. RESTORIS PST/TFS TOTAL HIP SYSTEM 10/31/2014
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