MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP; 1LYR 14FR 10ML 100%SILI UM TRAY

Catalog Number DYND160814

Device Problem Fluid/Blood Leak (1250)

Patient Problem Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)

Event Date 07/07/2023

Event Type  Injury  

Event Description

According to the facility on 07/07/2023 the foley catheter balloon was noted to be leaking.

Manufacturer Narrative

According to the facility on 07/07/2023, the foley catheter balloon was noted to be leaking.Per the facility the catheter was removed from the patient and a new foley catheter was placed.Sample requested to be returned for evaluation.No additional information is available at this time.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.

• Type of Device: 1LYR 14FR 10ML 100%SILI UM TRAY
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093
• Manufacturer Contact: justin herrmann ; three lakes drive; northfield, IL 60093
• MDR Report Key: 17396451
• MDR Text Key: 319835161
• Report Number: 1417592-2023-00317
• Device Sequence Number: 1
• Product Code: OHR
• UDI-Device Identifier: 10884389287408
• UDI-Public: 10884389287408
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 07/26/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/26/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Catalogue Number: DYND160814
• Device Lot Number: (10) 23CB0787
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/17/2023
• Date Manufacturer Received: 07/07/2023
• Was Device Evaluated by Manufacturer?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Other