MAUDE Adverse Event Report: Medline Industries, LP MEDLINE; STETHOSCOPE,SPRAGUE RAPPAPORT,BLACK

Catalog Number	MDS926301
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/12/2024
Type of Reportable Event	Malfunction

• Brand Name: MEDLINE
• Common Device Name: STETHOSCOPE,SPRAGUE RAPPAPORT,BLACK
• Manufacturer (Section D): Medline Industries, LP; three lakes drive; northfield IL 60093 -275
• Manufacturer Contact: arthem smalyukh ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50906374
• Report Number: 1417592-2026-51674
• Device Sequence Number: 9287736
• Product Code: LDE
• UDI-Device Identifier: 00080196717067
• UDI-Public: 00080196717067
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/18/2026

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
• Device Catalogue Number: MDS926301
• Device Lot Number: 65123070001
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 01/19/2024
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/12/2024
• Initial Report FDA Received Date: 09/26/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown