FDA Adverse Event Injury Summary report: N

WILLOW WEARABLE BREAST PUMP

MDR report key: 10319493 · Received July 24, 2020

Report

Report Number
3012759464-2020-00008
Event Type
Injury
Date Received
July 24, 2020
Date of Event
November 24, 2019
Report Date
July 24, 2020
Manufacturer
EXPLORAMED NC7, INC.
Product Code
HGX
UDI-DI
00858298006446
PMA / PMN Number
K191577
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER REPORTED MASTITIS WHICH WAS TREATED BY PRESCRIBED ANTIBIOTICS. A PRIMARY CAUSE OF MASTITIS IS MILK STASIS WITHIN THE BREAST, PROVIDING A MEDIUM FOR BACTERIAL GROWTH. THERE ARE A VARIETY OF RISK FACTORS FOR MASTITIS, INCLUDING MISSED OR RESTRICTED FEEDINGS, BREAST ENGORGEMENT, RESTRICTION FROM TIGHT BRA/ CLOTHING, PRONE SLEEPING POSITION, MATERNAL STRESS, EXCESSIVE FATIGUE, AND MALNUTRITION. MASTITIS IS USUALLY A BENIGN, SELF-LIMITING CONDITION, WITH FEW CONSEQUENCES TO THE INFANT AND INCIDENCE RANGING FROM 4-27%. 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 NONCONFORMANCES WERE NOTED IN THE PRODUCTION OF THIS DEVICE. BASED ON THE INFORMATION PROVIDED, IT CANNOT BE DEFINITIVELY CONCLUDED THAT THE WILLOW WEARABLE BREAST PUMP CAUSED OR CONTRIBUTED TO THE INCIDENT OF MASTITIS. WORLD HEALTH ORGANIZATION, MASTITIS CAUSES & MANAGEMENT, 2002. SPENCER JP, MANAGEMENT OF MASTITIS IN BREASTFEEDING WOMEN, AMERICAN FAMILY PHYSICIAN. 2008; 78 (6): 727-732. MICHIE C, THE CHALLENGE OF MASTITIS. ARCH DIS CHILD. 2003: 88, 818-821. FOXMAN B, LACTATION MASTITIS: OCCURRENCE AND MEDICAL MANAGEMENT AMONG 946 BREASTFEEDING WOMEN IN THE UNITED STATES. AM J EPIDEMIOL, 155 (2) 2002. WAMBACH, KAREN, AND JAN RIORDAN. BREASTFEEDING AND HUMAN LACTATION. 5TH ED., JONES & BARTLETT LEARNING, 2016.

Description of Event or Problem · 1

THE CUSTOMER REPORTED TO WILLOW CUSTOMER CARE ON 27 DEC 2019 THAT WILLOW WAS NOT EMPTYING HER BREASTS FULLY AND SHE HAD DEVELOPED MASTITIS AND WAS TREATED WITH ANTIBIOTICS. THE CUSTOMER REPORTED THAT SHE WENT TO THE EMERGENCY ROOM MULTIPLE TIMES ((B)(6) 2019 AND (B)(6) 2019) AND THAT ONE OF HER ANTIBIOTIC TREATMENTS CAUSED ANAPHYLAXIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
787863 WILLOW WEARABLE BREAST PUMP POWERED BREAST PUMP HGX EXPLORAMED NC7, INC. PDW48 00858298006446

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention