MAUDE Adverse Event Report: INFUTRONIX, LLC NIMBUS II PLUS AMBULATORY INFUSION PUMP

Model Number	NIMBUS II PLUS
Medical Device Problem Code	Power Problem (3010)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/26/2023
Type of Reportable Event	Malfunction
Event or Problem Description
Infutronix received a report that the patient experienced a power off and called support to attempt to resume infusion.There was no harm to the patient.No further details were provided.The medication is unknown.
Additional Manufacturer Narrative
The caller indicated that the pump had powered down and was calling to get help resuming the infusion.Support was able to confirm the reported issue while troubleshooting with the caller.However, the infusion could not be resumed but the caller was instructed on how to power off the pump and engage the blue clamp.The caller was instructed to follow-up with the infusion center promptly.This event could initially not be investigated further since the pump was not available for evaluation.Subsequently, on 11-jul-2024, the pump was returned to infutronix for investigation.The results of the investigation are not yet available.However, a follow-up report will be submitted once the investigation is completed.

• Brand Name: NIMBUS II PLUS AMBULATORY INFUSION PUMP
• Common Device Name: AMBULATORY INFUSION PUMP
• Manufacturer (Section D): INFUTRONIX, LLC; 177 pine street; natick MA 01760 1331
• Manufacturer (Section G): INFUTRONIX, LLC; 177 pine street; natick MA 01760 1331
• Manufacturer Contact: frederick lee ; 177 pine street; natick, MA 01760-1331 ; 5086502008
• MDR Report Key: 19956727
• Report Number: 3011581906-2024-00618
• Device Sequence Number: 12957934
• Product Code: FRN
• UDI-Device Identifier: 00817170020161
• UDI-Public: 00817170020161
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K153193
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer,Health Professional,Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Remedial Action: Recall
• Type of Report: Initial
• Report Date (Section B): 08/09/2024

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: Lay User/Patient
• Device Model Number: NIMBUS II PLUS
• Device Catalogue Number: NIMBUS J
• Device Lot Number: 2206213120
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/11/2024
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/11/2024
• Initial Report FDA Received Date: 08/09/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/21/2022
• 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
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: Z-1285-2024
• Patient Sequence Number: 1
• Patient Sex: Unknown