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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
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138 records meeting your search criteria returned- Product Code: KDQ Product Problem: Fluid/Blood Leak Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
TELEFLEX MEDICAL PE ADULT-PED WET LF 6/CS 11/09/2022
ATRIUM MEDICAL CORPORATION DRAINS OCEAN SINGLE 09/15/2022
ATRIUM MEDICAL CORPORATION OCEAN 09/13/2022
TELEFLEX INCORPORATED CHEST TUBE CANNISTER 06/16/2022
TELEFLEX INCORPORATED PLEUR-EVAC 06/06/2022
TELEFLEX INCORPORATED BOTTLE, COLLECTION, VACUUM 06/06/2022
CARDINAL HEALTH THORA SEAL 3 12/08/2021
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 11/11/2021
TELEFLEX MEDICAL PE ADULT-PED DRY/ WET LF 6/CS 10/21/2021
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 09/21/2021
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