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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
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18 records meeting your search criteria returned- Product Code: CAC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
HAEMONETICS, INC. CELL SAVER® ELITE® PLUS AUTOTRANSFUSION 05/10/2022
HAEMONETICS, INC. CELL SAVER® ELITE® PLUS AUTOTRANSFUSION 05/09/2022
HAEMONETICS, INC. CELL SAVER® ELITE® PLUS AUTOTRANSFUSION 12/03/2021
ATRIUM MEDICAL CORPORATION DRAINS OASIS SINGLE 09/25/2021
ATRIUM MEDICAL CORPORATION DRAINS OASIS SINGLE 04/12/2021
ATRIUM MEDICAL CORPORATION DRAINS OASIS SINGLE 04/12/2021
TERUMO BCT COBE 2991 10/07/2020
HAEMONETICS CORPORATION CELL SAVER ELITE AUTOTRANSFUSION SYSTEM 07/09/2020
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 04/27/2020
ATRIUM MEDICAL CORPORATION OCEAN CHEST DRAIN 04/27/2020
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