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

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ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. EXPLOR IMPLANT LOCKING SCREW 12/10/2019
ZIMMER BIOMET, INC. UNKNOWN STEM 12/10/2019
ACUMED LLC PROSTHESIS, ELBOW, HEMI-, RADIAL: STEM 08/29/2019
ACUMED LLC ARH SOLUTIONS HEAD 28MM, LEFT 08/29/2019
ACUMED LLC ARH SLIDE-LOC¿ NECK +1MM 08/29/2019
ZIMMER BIOMET, INC. EXPLOR 12X24 MM IMPLANT HEAD 03/21/2019
STRYKER GMBH LAT ASSEMBLY, RAD STEM HEAD IMPLANT, SIZ 12/13/2018
STRYKER CORP. STRYKER RADIAL HEAD REPLACEMENT 12/06/2018
STRYKER GMBH LATERAL ASSEMBLY, RADIAL HEAD IMPLANT, S 10/24/2018
STRYKER GMBH LATERAL ASSEMBLY, RADIAL HEAD IMPLANT, S 09/27/2018
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