MAUDE Adverse Event Report: MEDELA LLC PUMP IN STYLE ADVANCED BREAST PUMP BACKPACK; PUMP, BREAST, POWERED

Model Number 57060/9207041

Device Problem Crack (1135)

Patient Problem No Information (3190)

Event Date 03/31/2017

Event Type  malfunction  

Manufacturer Narrative

The product involved in the complaint was not returned for evaluation/investigation at this time.Therefore, no conclusions can be made as to the cause of the event.The cause of the breach in the 9207041 transformer has not been determined at this time.It is currently being investigated under ir14-(b)(4).

Event Description

The customer reported to customer service on (b)(6) 2017, that the power cord to her pump in style backpack had a crack and was opened.

• Brand Name: PUMP IN STYLE ADVANCED BREAST PUMP BACKPACK
• Type of Device: PUMP, BREAST, POWERED
• Manufacturer (Section D): MEDELA LLC; 1101 corporate dr; mchenry IL 60050
• Manufacturer (Section G): MEDELA LLC; 1101 corporate dr; mchenry IL 60050
• Manufacturer Contact: robert sokolowski ; 1101 corporate drive; mchenry, IL 60050
• MDR Report Key: 6481371
• MDR Text Key: 72783273
• Report Number: 1419937-2017-00095
• Device Sequence Number: 1
• Product Code: HGX
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K031614
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 04/11/2017

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 Operator: Lay User/Patient
• Device Model Number: 57060/9207041
• Device Catalogue Number: 57060/9207041
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Distributor Facility Aware Date: 03/31/2017
• Initial Date Manufacturer Received: 03/31/2017
• Initial Date FDA Received: 04/11/2017
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1