MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE IRIS URETERAL KIT; LIGHT, CATHETER, FIBEROPTIC, GLASS, URETERAL

Catalog Number 0220180518

Device Problems Use of Device Problem (1670); Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Blood Loss (2597)

Event Date 05/27/2020

Event Type  Injury  

Manufacturer Narrative

The device manufacturer date is not known at this time.However, should it become available it will be provided in future reports.

Event Description

It was reported that the surgeon cut across the patient ureter and the procedure was cancelled due to bleeding during the catheter insertion.

Manufacturer Narrative

This complaint investigation was closed based on the device not received, therefore the reported failure mode was not confirmed.In the event that the device is received, the complaint will be reopened and the investigation will be updated with new results.Alleged failure: bleeding during the catheter insertion probable root cause: incorrect device dimensions.Incorrect catheter durometer.Incorrect device used.Manufacturing nonconformity.(e.G.Incorrect hydrophilic coating).Improper storage or shipping conditions the reported failure mode will be monitored for future reoccurrence.The device manufacturer date is not known at this time.H3 other text : 81.

Event Description

Update: it was reported that there was ureteral bleeding during the catheter insertion requiring treatment.It was reported that the surgeon cut across the patient ureter and the procedure was cancelleed due to bleeding during the catheter insertion.

• Brand Name: IRIS URETERAL KIT
• Type of Device: LIGHT, CATHETER, FIBEROPTIC, GLASS, URETERAL
• Manufacturer (Section D): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• MDR Report Key: 10180910
• MDR Text Key: 196005834
• Report Number: 0002936485-2020-00241
• Device Sequence Number: 1
• Product Code: FCS
• UDI-Device Identifier: 37613327174817
• UDI-Public: 37613327174817
• Combination Product (y/n): N
• PMA/PMN Number: K151243
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 08/25/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/22/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 0220180518
• Device Lot Number: 4297062
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 05/27/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other