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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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14 records meeting your search criteria returned- Product Code: GCJ Patient Problem: Unintended Radiation Exposure Report Date From: 01/1/2018
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ManufacturerBrand NameDate Report Received
DAVIS & GECK CARIBE LTD VERSAONE 05/10/2023
DAVIS & GECK CARIBE LTD UNKNOWN TROCAR DEVICE 02/21/2023
COVIDIEN LP LLC NORTH HAVEN LAPRO-CLIP 01/13/2023
US SURGICAL PUERTO RICO MULTIFIRE ENDO HERNIA 09/23/2022
DAVIS & GECK CARIBE LTD VERSAONE 07/22/2022
DAVIS & GECK CARIBE LTD VERSAONE 04/12/2022
DAVIS & GECK CARIBE LTD MULTIFIRE VERSATACK 03/23/2022
US SURGICAL PUERTO RICO UNKNOWN PROTACK 03/02/2022
US SURGICAL PUERTO RICO PROTACK 12/29/2021
US SURGICAL PUERTO RICO STEP 10/06/2021
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