MAUDE Adverse Event Report: EXPLORAMED NC7, INC. WILLOW WEARABLE BREAST PUMP; POWERED BREAST PUMP

Model Number	PDW48
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	06/06/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The customer reported thrush which was treated by a doctor prescribed antifungal medication.Thrush is caused by a yeast fungus.1 yeast grows in moist, warm environments.Risk of developing thrush can be increased by recent course of antibiotics 1, cracked or damaged nipples 1, oral contraceptives or steroids 1, clothing not designed for breastfeeding that traps moisture, 2, and hot, humid conditions, 2.The willow device has not yet been returned to exploramed nc7 for evaluation.However, a manufacturing review was conducted on the device history record and no nonconformance's were noted in the production of this device.Based on the information provided, it cannot be definitively concluded that the willow breast pump caused or contributed to this incident of thrush.La leche league international, https://www.Llli.Org/breastfeeding-info/thrush/.Healthline, nipple thrush and breastfeeding, https://www.Healthline.Com/health/nipple-thrush # takeaway.
Event or Problem Description
The customer reported to willow customer care on (b)(6) 2020 that she had been diagnosed with thrush from a lactation specialist and then received prescription antifungal from her ob/gyn.She took a 14 day oral dose of fluconazole and a topical antifungal cream.

• Brand Name: WILLOW WEARABLE BREAST PUMP
• Common Device Name: POWERED BREAST PUMP
• Manufacturer (Section D): EXPLORAMED NC7, INC.; 1975 w. el camino real; suite 306; mountain view,
• MDR Report Key: 10312942
• Report Number: 3012759464-2020-00007
• Device Sequence Number: 11000777
• Product Code: HGX
• UDI-Device Identifier: 00858298006446
• UDI-Public: (01)00858298006446(11)200415
• Combination Product (Y/N): N
• PMA/510(K) Number: K191577
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/22/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: No Information
• Device Model Number: PDW48
• Device Catalogue Number: PDW48
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/22/2020
• Initial Report FDA Received Date: 07/23/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention