MAUDE Adverse Event Report: BALT EXTRUSION MAGIC INFUSION CATHETER

Model Number MAGIC1,2FM

Device Problem Material Rupture (1546)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 12/29/2022

Event Type  malfunction  

Manufacturer Narrative

Balt usa reference (b)(4).Note: this complaint file is being reported late as part of a corrective action following an fda inspection.After a review of historical complaint files, it was determined that for this compaint the claimed malfunction did not lead to a death or serious injury.However, based on post market surveillance data and the intial information that was reported to balt, the same malfunction has led to a serious injury or death in a separate incident which was already mdr reported (remains as an unlikely probability according to risk analysis document).Further analysis pending final investigation results from legal manufacture.The submission of this report or related information to the fda, and its release by fda, does not reflect a conclusion by the party submitting this report of the fda that the report or related information is an admission that the manufacturer, their employees, or the device caused or contributed to the reportable event.

Event Description

It was reported that: "physician was doing a spine avm case.Plan was to inject glu with the help of magic micro catheter.He prepared well magic & hybrid outside of the table and started the procedure.He found that during the navigation, hybrid wire was coming out from the proximal part of its tip.He took it out and checked it on table then he found that micro catheter had a tiny whole, so he discarded it and took another magic and completed the procedure." incident report form received for this complaint indicated no patient injury was sustained.

• Brand Name: MAGIC INFUSION CATHETER
• Type of Device: MAGIC
• Manufacturer (Section D): BALT EXTRUSION; 10 rue de la croix vigneron; montmorency, 95160 ; FR 95160
• Manufacturer Contact: david vu ; 29 parker; irvine, CA 92618 ; 9497881443
• MDR Report Key: 17573088
• MDR Text Key: 321663754
• Report Number: 3014162263-2023-00047
• Device Sequence Number: 1
• Product Code: KRA
• UDI-Device Identifier: 03700481335451
• UDI-Public: (01)03700481335451(11)220627(17)270528(10)00489092
• Combination Product (y/n): N
• Reporter Country Code: IN
• PMA/PMN Number: K023351
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 08/08/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/18/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: MAGIC1,2FM
• Device Lot Number: 00489092
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 01/03/2023
• Was Device Evaluated by Manufacturer?: No
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1