MAUDE Adverse Event Report: ABBOTT VASCULAR MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM; VALVE REPAIR

Catalog Number	CDS0501
Medical Device Problem Codes	Off-Label Use (1494); Migration (4003)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	07/10/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The mitraclip remains in patient.Investigation is not yet complete.A follow-up report will be submitted with all additional relevant information.The other additional cds0501 referenced in b5 is filed under a separate medwatch report number.G9: exemption number e2019001-permits numbering sequence to begin with 10000, to avoid duplication of report numbers due to process transition.There may be gaps in numbering for reports submitted during the transition period.Na.
Event or Problem Description
This is filed for partial clip movement after deployment (cds0501/90416u111).It was reported that this was a mitraclip procedure to treat functional mitral regurgitation (mr) with a grade of 4.A mitraclip was advanced and implanted in the mitral valve, successfully reducing mr to 1.The procedure continued to treat tricuspid regurgitation (tr) with a grade of 4.A mitraclip (cds0501 lot 90416u111) was advanced and deployed, reducing tr to 1.However, on fluoroscopy the clip looked unstable and grasped only 4mm of the anterior leaflet and 6mm of the septal leaflet.After deployment both leaflets were fully captured, however movement of the clip was too erratic.It was decided to implant a second clip to stabilize this clip.Visualization during the introduction of the cds was difficult due to the position of the valve.A mitraclip (cds0501 lot 90416u110) was advanced with a 90 degree miss-key to the steerable guide catheter (sgc).The clip was unable to move as expected and it was decided to retry with a miss-key of 180 degrees.The clip delivery system (cds) had a better response to 180 degree mis-key, however it was difficult to move.The cds was retracted, however the tip of the clip got caught in tissue although it was not clear where or what tissue.Troubleshooting for chordal entanglement was performed but was unable to be freed.The clip was able to be deployed correctly on the septal and anterior leaflets.During removal of the delivery catheter (dc), fluoroscopy showed it jumped back.The sgc and cds were retracted together.Once outside the patient anatomy, it was noted that a tissue from the patient was grasped onto the base of the dc radiopaque ring.Post-procedure tr was 1.This issue reportedly caused a clinically significant delay.No additional information was provided.
Additional Manufacturer Narrative
The device was not returned for analysis.A review of the lot history record identified no manufacturing nonconformities issued to the reported lot that would have contributed to the reported event.Additionally, a review of the complaint history did not identify similar incidents reported from this lot.All available information was investigated, reported poor imaging appear to be due to patient anatomy.Furthermore, reported partial clip movement(migration) appears due to a combination of challenging patient morphology/pathology and user technique/procedural conditions.The patient selection (off label use) was associated with the use of the mitraclip device on the tricuspid valve, which is considered an off-label use of the device.There is no indication of a product issue with respect to manufacture, design or labeling.Exemption number e2019001.

• Brand Name: MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM
• Common Device Name: VALVE REPAIR
• Manufacturer (Section D): ABBOTT VASCULAR; 26531 ynez rd.; temecula CA 92591 4628
• MDR Report Key: 8800869
• Report Number: 2024168-2019-10129
• Device Sequence Number: 221384
• Product Code: NKM
• UDI-Device Identifier: 08717648216800
• UDI-Public: 08717648216800
• Combination Product (Y/N): N
• Initial Reporter Country: MX
• PMA/510(K) Number: P100009
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 09/10/2019

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 04/16/2020
• Device Catalogue Number: CDS0501
• Device Lot Number: 90416U111
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 07/10/2019
• Supplement Date Received by Manufacturer: 09/05/2019
• Initial Report FDA Received Date: 07/17/2019
• Supplement Report FDA Received Date: 09/10/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 1 IMPLANTED MITRACLIPS; STEERABLE GUIDE CATHETER
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 79 YR
• Patient Weight: 60