MAUDE Adverse Event Report: OSCOR INC. INTRODUCER KIT FOR IMPELLA®; INTRODUCER, CATHETER

Model Number 0052-3025

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Cardiac Arrest (1762); Blood Loss (2597)

Event Date 02/22/2020

Event Type  Injury  

Manufacturer Narrative

The device was used in the treatment.The device was discarded and not returned for analysis.There was no specific performance related failure reported by the user.The device history record was reviewed to confirm that the device passed all applicable inprocess and final inspections.No further investigation is required.Based on the investigation, a capa is not required as as findings did not identify a design, labeling or manufacturing nonconformity.The event will be re-evaluated if additional information becomes available.No further follow-up is required.

Event Description

It was reported that during cardiogenic shock procedure, there was bleeding at the insertion site.User reported that there was no issue with introducer.They noticed excessive bleeding after giving heparin for anticoagulation once the sheath was in.The first cp was placed had excessive bleeding in the right groin.Then the second cp was placed in the left groin once the first cp was removed from the sheath.Patient loss 800ml blood.Two (2) units of red blood cells (rbcs) were given and gore sheath was placed for hemostasis in right groin and new cp in left groin.The sheath was sutured to the skin.The bleeding caused a delay in putting the rp in, which we never got to because of the condition of the patient.Patient was very sick.Patient expired on 22nd february from cardiac arrest.The patient was in cardiac standstill.There was no product malfunction reported.Device was discarded.No other information is available.

Manufacturer Narrative

The following sections were updated in follow-up.B4,d4,g4,g7,h2,h10.Correction : d4 : expiration date corrected oscor inc.Is submitting the above report to comply with 21 cfr part 803, the medical device reporting regulation.The report is based upon information obtained by oscor inc.Which the company may not have been able to investigate or verify prior to the date the report was required by fda.This report does not constitute an admission that the device, oscor inc., or its employees, caused or contributed to the event described in this report.Nor does this report reflect a conclusion by fda, oscor inc., or its employees, that the report constitutes an admission that the device, oscor inc., or its employees caused or contributed to the event described in this report.

• Brand Name: INTRODUCER KIT FOR IMPELLA®
• Type of Device: INTRODUCER, CATHETER
• Manufacturer (Section D): OSCOR INC.; 3816 desoto blvd.; palm harbor, fl
• MDR Report Key: 9850021
• MDR Text Key: 186805972
• Report Number: 1035166-2020-00021
• Device Sequence Number: 1
• Product Code: DYB
• UDI-Device Identifier: 00885672009793
• UDI-Public: 00885672009793
• Combination Product (y/n): N
• PMA/PMN Number: K122084
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor
• Type of Report: Initial,Followup
• Report Date: 03/19/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/18/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 10/01/2022
• Device Model Number: 0052-3025
• Device Catalogue Number: 0052-3025
• Device Lot Number: C1-17964
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 03/18/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 28 YR