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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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425 records meeting your search criteria returned- Product Code: KDI Product Problem: Leak/Splash Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAFLEX SETS (ST) 11/18/2022
BAXTER HEALTHCARE CORPORATION REVACLEAR 400 11/16/2022
BAXTER HEALTHCARE CORPORATION REVACLEAR 400 11/15/2022
BAXTER HEALTHCARE CORPORATION REVACLEAR 11/02/2022
BAXTER HEALTHCARE CORPORATION REVACLEAR 10/26/2022
BAXTER HEALTHCARE CORPORATION PRISMAX ACCESSORY, AUTO EFFLUENT 10/25/2022
BAXTER HEALTHCARE CORPORATION PHOENIX 10/25/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX SET (M) 10/18/2022
BAXTER HEALTHCARE CORPORATION REVACLEAR 10/04/2022
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 09/30/2022
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