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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
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90 records meeting your search criteria returned- Product Code: PAO Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE GLENOSPHERE 11/06/2020
ENCORE MEDICAL L.P. ALTIVATE SHOULDER 05/31/2019
ENCORE MEDICAL L.P. ALTIVATE SHOULDER 03/21/2019
ENCORE MEDICAL L.P. ALTIVATE SHOULDER 03/15/2019
ZIMMER BIOMET, INC. COMP RVRS SHLDR GLNSP STD 36MM 01/07/2019
ENCORE MEDICAL L.P. ALTIVATE ANATOMIC SHOULDER 12/14/2018
ZIMMER BIOMET, INC. E1 44-36 STD +3 HMRL BRG 10/03/2018
ZIMMER BIOMET, INC. COMP RVSR SHLDR GLNSP +3 36MM 08/31/2018
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE GLENOSPHERE STANDA 08/15/2018
ZIMMER BIOMET, INC. COMPREHENSIVE E1 RETENTIVE +3 MM HUMERAL 08/15/2018
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