MAUDE Adverse Event Report: SISTEMAS MEDICOS ALARIS S.A. DE C.V. BD ALARIS PUMP MODULE SMARTSITE INFUSION SET; INTRAVASCULAR ADMINISTRATION SET

Catalog Number 11419365

Device Problem Excess Flow or Over-Infusion (1311)

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

Event Date 10/25/2023

Event Type  malfunction  

Event Description

It was reported that bd alaris pump module smartsite infusion set over infused.The following information was received by the initial reporter with the following verbatim: in the bldg d r&d lab, an infusion with an alaris system set incorporated with a distal manifold (model: 11419365), resulted in an over infusion as the infusion was initiated on 1 out of 3 sets tested.The infusion was programmed to run at 0.1 ml/hr for 96 hours as stated in test protocol 10000421654 date of event: (b)(6) 2023.Hold for wh 12.19.

Manufacturer Narrative

H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.

Manufacturer Narrative

It was reported by customer an infusion resulted in an over infusion.Five photos were received for quality investigation.The photos received show a test that was conducted by bd r&d to determine the accuracy of the flow rate.The following is the description of the test conducted by bd r&d.In the bldg d r&d lab, an infusion with an alaris system set incorporated with a distal manifold (model: 11419365), resulted in an over infusion as the infusion was initiated on 1 out of 3 sets tested.The infusion was programmed to run at 0.1 ml/hr for 96 hours as stated in test protocol (b)(4).A sample was then sent to vernon hills for quality testing in the ipd lab.The sample of material number 11419365 was primed with water and connected to an alaris pump to conduct a simulated infusion at a rate of 0.1 ml/hr for 100 hours.At the end of the infusion, the dispensed amount of liquid was exactly 10 ml.The testing could not validate the results from the previous testing conducted.The complaint of flow accuracy could not be confirmed, and no under infusion or over infusion was determined.A root cause for the reported failure was not determined because a failure was not verified.A device history record review for model 11419365 lot number 23075082 was performed.The search showed that a total of (b)(4) units in 1 lot number was built on 04jul2023.There were no quality notifications issued for the failure mode reported by the customer during the production build of this set.This incident has been added to our database of reported incidents.Our business team regularly reviews the collected data for identification of emerging trends.

Event Description

No additional information was provided.Material#: 11419365, batch number#: 23075082.It was reported by customer that in the bldg d r&d lab, an infusion with an alaris system set incorporated with a distal manifold (model: 11419365), resulted in an over infusion as the infusion was initiated on 1 out of 3 sets tested.The infusion was programmed to run at 0.1 ml/hr for 96 hours as stated in test protocol (b)(4).Verbatim#: rcc received a complaint via email.Email(s) attached.In the bldg d r&d lab, an infusion with an alaris system set incorporated with a distal manifold (model: 11419365), resulted in an over infusion as the infusion was initiated on 1 out of 3 sets tested.The infusion was programmed to run at 0.1 ml/hr for 96 hours as stated in test protocol (b)(4).Date of event: 25oct2023.

• Brand Name: BD ALARIS PUMP MODULE SMARTSITE INFUSION SET
• Type of Device: INTRAVASCULAR ADMINISTRATION SET
• Manufacturer (Section D): SISTEMAS MEDICOS ALARIS S.A. DE C.V.; blvd. insurgentes no. 20351; parque industrial el florido; tijuana
• Manufacturer (Section G): SISTEMAS MEDICOS ALARIS, S.A. DE C.V.; blvd. insurgentes no. 20351; parque industrial el florido; tijuana
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 18322600
• MDR Text Key: 330966021
• Report Number: 9616066-2023-02406
• Device Sequence Number: 1
• Product Code: FPA
• UDI-Device Identifier: 50885403234734
• UDI-Public: (01)50885403234734
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K944320
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 12/11/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/13/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Device Catalogue Number: 11419365
• Device Lot Number: 23075082
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/05/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 07/04/2023
• Is the Device Single Use?: Yes
• Type of Device Usage: Initial
• Patient Sequence Number: 1