MAUDE Adverse Event Report: COOK INC PERFORMER INTRODUCER; DYB INTRODUCER, CATHETER

Model Number	G27022
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	09/01/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Concomitant medical products: guire wire terumo rf-ga35153m angled 0.035; ander-bear hugger blanket model 530 pediatric long; pigtail terumo straight pigtail rq-4sps04mg; mp-532-506-5f-80cm 406; hnb4.1-35-80-p-ns-jr2.5; rcfn-4.0-18-5.5-ra1.5; rcfn-5.0-18-5.5-ra1.5 pma/510(k) number = pre-amendment.This report includes information known at this time.A follow-up report will be submitted should additional relevant information become available.
Event or Problem Description
As reported, during an unknown procedure, a performer introducer leaked between the hub and sheath.Blood loss was reported; however, it is unknown if any intervention was required to treat blood loss.No additional procedures were required.Additional information has been requested, but is unavailable at this time.
Event or Problem Description
Additional information was received.The procedure involved a pediatric patient of unknown age and gender.
Additional Manufacturer Narrative
Blank fields on this form indicate the information is unknown, unavailable, or unchanged.Additional information: b5, d10.This report includes information known at this time.A follow-up report will be submitted should additional relevant information become available.This report is required by the fda under 21 cfr part 803 and is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement contained herein is intended to be an admission that any cook device is defective or malfunctioned, that a death or serious injury occurred, nor that any cook device caused, contributed to, or is likely to cause or contribute to a death or serious injury if a malfunction occurred.
Event or Problem Description
No additional information regarding the patient and/or event has been received since the previous medwatch report was sent.
Additional Manufacturer Narrative
Blank fields on this form indicate the information is unknown, unchanged, or unavailable.Summary of event: as reported, during an unknown procedure involving a pediatric patient of unknown age and gender, a performer introducer leaked between the hub and sheath.Blood loss was reported; however, it is unknown if any intervention was required to treat blood loss.No additional procedures were required.Additional information was requested; however, was not received.Investigation evaluation: reviews of the complaint history, device history record, drawing, documentation, instructions for use (ifu), manufacturing instructions, quality control, and specifications were conducted during the investigation.A visual inspection and functional test of the complaint device was also conducted.The complaint device was returned to cook for investigation.The device was flushed, and a leak was noted where the tubing enters check-flo.The check-flo and cap were disassembled, and a tear was found on the flare.A document-based investigation evaluation was performed.Two possibly related non-conformances were noted on the lot; however, all affected devices were reworked per specification.There have been no other reported complaints for this lot number.Evidence from the complaint file, device history record, complaint history, validations, manufacturing documents, and device failure analysis suggests that the device was manufactured to specification.There is no evidence of nonconforming devices from the complaint lot in-house or in the field.The product ifu instructs the user to inspect the product to ensure no damage has occurred upon removal from the package.Based on the information provided and the results of the investigation, cook has concluded that a component failure caused this event.The risk analysis for this failure mode was reviewed and no additional escalation was required.The appropriate personnel have been notified and cook will continue to monitor for similar events.This report is required by the fda under 21 cfr part 803 and is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement contained herein is intended to be an admission that any cook device is defective or malfunctioned, that a death or serious injury occurred, nor that any cook device caused, contributed to, or is likely to cause or contribute to a death or serious injury if a malfunction occurred.

• Brand Name: PERFORMER INTRODUCER
• Common Device Name: DYB INTRODUCER, CATHETER
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 10520557
• Report Number: 1820334-2020-01658
• Device Sequence Number: 19634149
• Product Code: DYB
• UDI-Device Identifier: 00827002270220
• UDI-Public: (01)00827002270220(17)230217(10)10301484
• Combination Product (Y/N): N
• Initial Reporter Country: BE
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 11/17/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 02/17/2023
• Device Model Number: G27022
• Device Catalogue Number: RCFN-4.0-18-5.5-RA1.5
• Device Lot Number: 10301484
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/18/2020
• Initial Date Received by Manufacturer: 09/01/2020
• Supplement Date Received by Manufacturer: 09/16/2020; 11/11/2020
• Initial Report FDA Received Date: 09/11/2020
• Supplement Report FDA Received Date: 10/13/2020; 11/17/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1