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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
BIOMET ORTHOPEDICS ARCOM XL 44-36 STD +3 HMRL BRG 04/27/2015
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE SHLDR GLENOSPHERE 02/27/2015
BIOMET ORTHOPEDICS ARCOM XL 44-36 STD +3 HUMERAL BEARING 02/27/2015
BIOMET ORTHOPEDICS COMPREHENSIVE REVERSE HUMERAL TI TRAY 44 02/27/2015
BIOMET ORTHOPEDICS COMP RVRS SHLDR GLNSP STD 41MM 01/28/2015
BIOMET ORTHOPEDICS COMP RVRS SHLDR GLNSP STD 36MM 12/11/2014
BIOMET ORTHOPEDICS ARCOM XL 44-36 STD HMRL BRNG 09/02/2014
BIOMET ORTHOPEDICS COMP RVRS SHLDR GLNSP STD 36MM 09/02/2014
BIOMET ORTHOPEDICS COMP RVRS SHLDR GLNSP +6 41MM 06/23/2014
BIOMET ORTHOPEDICS COMP RVSR SHLDR GLNSP +3 36MM 05/29/2014
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