MAUDE Adverse Event Report: SMITHS MEDICAL ASD, INC. LEVEL 1 FLUID WARMER; DEVICE, WARMING, BLOOD AND PLASMA

Model Number	D-60HL
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
Information received a smiths medical fluid warming|level 1 trauma fast flow disposables d-60hl was leaking.No patient involvement.
Additional Manufacturer Narrative
Device evaluation- two devices were returned for evaluation.The visual inspection of the devices showed no obvious defects.The devices were given functional testing; both were found to allow for priming and warming with no leakage occurring.The reported issue could not be confirmed with the returned devices.The manufacturing process includes the following mitigation's against leakage: 100% pressure testing after assembly of drip chamber and iv spike, 100% pressure testing after assembly of the heat exchanger.In addition, the devices are sampled at regular intervals for further testing and inspection.
Additional Manufacturer Narrative
Additional: d5.This mdr was generated under protocol (b)(4), as a result of warning letter cms# (b)(4).A product sample was received for evaluation.Visual and functional testing were performed.In image 1 a sample with a leak can be seen, however, it is not possible to determine where the leak is coming from according to the image provided.Samples received: two samples were received for evaluation; the samples were received decontaminated without its original package.Picture 2: visual inspection: the returned samples were visually inspected at a distance of 12 to 16 inches under normal conditions of illumination according to procedures.Results: visual inspection revealed that no damage, defects, or discrepancies were found in the sample.Picture three: functional test: the sample was test for leak by introducing water in the product.Results: the samples have passed the test successfully; thus, the failure mode report is not confirmed.Picture four sample one.Picture five sample two.Other analysis no other analysis was performed.Root cause cannot be determined since the complaint was not confirmed due to the fact the samples was tested and successfully passed.No actions are required since the complaint was not confirmed.

• Brand Name: LEVEL 1 FLUID WARMER
• Common Device Name: DEVICE, WARMING, BLOOD AND PLASMA
• Manufacturer (Section D): SMITHS MEDICAL ASD, INC.; 6000 nathan lane north; minneapolis MN 55442
• Manufacturer (Section G): SMITHS MEDICAL ASD, INC.; 6000 nathan lane north; parque internacional industria; minneapolis MN 55442
• Manufacturer Contact: jim vegel ; 6000 nathan lane north; minneapolis, MN 55442 ; 7633833310
• MDR Report Key: 12328488
• Report Number: 3012307300-2021-08488
• Device Sequence Number: 19534930
• Product Code: KZL
• UDI-Device Identifier: 20695085406003
• UDI-Public: 20695085406003
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: BK860023
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 02/24/2023

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 Expiration Date: 04/20/2025
• Device Model Number: D-60HL
• Device Catalogue Number: D-60HL
• Device Lot Number: 4114256
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/11/2021
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/19/2021
• Supplement Date Received by Manufacturer: 12/20/2021; 02/01/2023
• Initial Report FDA Received Date: 08/16/2021
• Supplement Report FDA Received Date: 01/20/2022; 02/23/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/04/2025
• 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: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown