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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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166 records meeting your search criteria returned- Product Code: FPA Product Problem: Tear, Rip or Hole in Device Packaging Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE - CALI PLEXITRON SOLUTION ADMINISTRATION SETS 07/12/2019
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 07/09/2019
CAREFUSION ALARIS NON VENTED BLOOD SET 06/13/2019
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 06/03/2019
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 05/29/2019
CAREFUSION ALARIS® PUMP MODULE ADMINISTRATION SET 05/23/2019
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 05/23/2019
CAREFUSION ALARIS PUMP MODULE SET 04/09/2019
BD (SUZHOU) UNSPECIFIED BD¿ CATHETER 03/29/2019
CAREFUSION ALARIS® PUMP MODULE ADMINISTRATION SET 03/27/2019
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