MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP Medline; TRAY,FOLEY,100% SILICONE,18FR,10ML,LF

Model Number DYND11520

Device Problem Burst Container or Vessel (1074)

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

Event Date 02/25/2023

Event Type  malfunction  

Manufacturer Narrative

According to the customer contact catheter "fell out or was leaking".Due to the reported event the foley catheter was replaced.No additional details were provided.A sample was requested to be returned for evaluation.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.

Event Description

Catheter fell out, or was leaking requiring replacement.

• Brand Name: Medline
• Type of Device: TRAY,FOLEY,100% SILICONE,18FR,10ML,LF
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093
• Manufacturer Contact: kelly zampella ; three lakes drive; northfield, IL 60093
• MDR Report Key: 16573923
• MDR Text Key: 311686871
• Report Number: 1417592-2023-00117
• Device Sequence Number: 1
• Product Code: OHR
• UDI-Device Identifier: 10080196997060
• UDI-Public: 10080196997060
• 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: 03/20/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/20/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Model Number: DYND11520
• Device Catalogue Number: DYND11520
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 03/02/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Other