MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION GREENFIELD; FILTER, INTRAVASCULAR, CARDIOVASCULAR

Model Number	43335
Medical Device Problem Code	Positioning Failure (1158)
Health Effect - Clinical Code	Injury (2348)
Date of Event	08/30/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
In (b)(6)1998 the patient underwent placement of a greenfield vena cava filter.In (b)(6) 2019 a computed tomography (ct) scan revealed the filter appeared to be in a satisfactory position, however there was an additional filter which did not deploy; identified within the right iliac vein.
Event or Problem Description
In (b)(6) 1998 the patient underwent placement of a greenfield vena cava filter.In (b)(6) 2019 a computed tomography (ct) scan revealed the filter appeared to be in a satisfactory position, however there was an additional filter which did not deploy; identified within the right iliac vein.

• Brand Name: GREENFIELD
• Common Device Name: FILTER, INTRAVASCULAR, CARDIOVASCULAR
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• MDR Report Key: 9938839
• Report Number: 2134265-2020-04708
• Device Sequence Number: 644446
• Product Code: DTK
• UDI-Device Identifier: 08714729070276
• UDI-Public: 08714729070276
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K964284
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 1998
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 08/13/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 01/01/2001
• Device Model Number: 43335
• Device Catalogue Number: 43335
• Device Lot Number: 0001266221
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/24/2020
• Supplement Date Received by Manufacturer: 07/22/2020
• Initial Report FDA Received Date: 04/08/2020
• Supplement Report FDA Received Date: 08/13/2020
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 61 YR