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NATURA Adverse Event — Malfunction (MDR 9618003-2020-10571)

NATURA Adverse Event — Malfunction (MDR 9618003-2020-10571) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NATURA; Generic name: PROTECTOR, OSTOMY; Manufacturer: CONVATEC DOMINICAN REPUBLIC INC.

DeviceNATURA
Generic namePROTECTOR, OSTOMY
ManufacturerCONVATEC DOMINICAN REPUBLIC INC
Report number9618003-2020-10571
Event typeMalfunction
Product problemN
Date received2020-04-28
Report sourceCONSUMER
NarrativeDEVICE 12 OF 20. BASED ON THE AVAILABLE INFORMATION, THIS EVENT IS DEEMED TO BE A REPORTABLE MALFUNCTION. THIS COMPLAINT HAS BEEN EVALUATED. NO LOT NUMBER IS AVAILABLE. A DETAILED INVESTIGATION OR BATCH REVIEW CANNOT BE CONDUCTED. THEREFORE, THIS EVALUATION WILL BE CLOSED. THIS ISSUE WILL BE MONITORED THROUGH THE POST MARKET PRODUCT MONITORING REVIEW PROCESS. TO DATE NO ADDITIONAL INFORMATION HAS
SourceopenFDA MAUDE (device adverse events)

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