MAUDE Adverse Event Report: MEDIVANCE -1725056 ARCTIC SUN® TEMPERATURE MANAGEMENT SYSTEM, TEMP OUT CABLE

Catalog Number	735-52
Medical Device Problem Code	Device Sensing Problem (2917)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/29/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the problems with temperature transmission from arctic sun device to monitor.Per follow up information received via mail on 03sep2025, device would be repaired in the hospital by crs.No patient involvement.
Additional Manufacturer Narrative
Initial facility reporter name: klinikum bremen-mitte ggmbh station modulbau intensiv 3028 the investigation is still in progress.Once the investigation is complete a supplemental report will be filed.All available udi information is being provided.H11: section a through f - the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
Additional Manufacturer Narrative
The initial reporter's facility name" (b)(6).The reported issue was confirmed.The root cause of the reported issue is a failed temperature out cable.Alarm 48 patient temperature out invalid present.Calibration is needed.Exchanged temperature out cable and performed a calibration.Tested the system with a simulator for the patient`s temperature.The evaluation found no other issues with the arcticsun performance.The complaint or reported issue was confirmed through other elements of the investigation to not be labeling or packaging related.A dhr review is not required as the lot number is unknown.No additional actions are needed.Corrections: d, e, h.Udi format updated with available product information per gudid.H11: sections a through f - the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.
Event or Problem Description
It was reported that the problems with temperature transmission from arctic sun device to monitor.Per follow up information received via mail on 03sep2025, device would be repaired in the hospital by crs.No patient involvement.
Event or Problem Description
It was reported that the problems with temperature transmission from arctic sun device to monitor.Per follow up information received via mail on 03sep2025, device would be repaired in the hospital by crs.No patient involvement.
Additional Manufacturer Narrative
Initial facility reporter name: (b)(6).The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.Correction: d.All available udi information is being provided.H11: section a through f: the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.

• Brand Name: ARCTIC SUN® TEMPERATURE MANAGEMENT SYSTEM, TEMP OUT CABLE
• Common Device Name: TEMP OUT CABLE
• Manufacturer (Section D): MEDIVANCE -1725056; 321 south taylor ave; suite 200; louisville CO 80027
• Manufacturer (Section G): MEDIVANCE -1725056; 321 south taylor ave; suite 200; louisville CO 80027
• Manufacturer Contact: xeeroy rada ; 8195 industrial blvd; covington, GA 30014 ; 7707846100
• MDR Report Key: 22963529
• Report Number: 1018233-2025-07457
• Device Sequence Number: 12827035
• Product Code: DWJ
• UDI-Device Identifier: 00801741080340
• UDI-Public: (01)00801741080340(11)121101
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K161602
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Health Professional,User Facility
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 01/12/2026

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
• Operator of Device: Health Professional
• Device Catalogue Number: 735-52
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/29/2025
• Supplement Date Received by Manufacturer: 01/08/2026; 01/12/2026
• Initial Report FDA Received Date: 09/04/2025
• Supplement Report FDA Received Date: 01/12/2026; 01/14/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/01/2012
• 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
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown