Double Pump Kit, Gen 3 (2S), White, 27mm PDW50Recalls & reported problems
Willow Innovations, Inc. · Double Pump Kit, Gen 3 (2S), White, 27mm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00858298006484), received between Aug 19, 2020 and Oct 2, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
Patient problems
- Injury1
- Skin Infection1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 2, 2020Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORTED TO WILLOW CUSTOMER CARE ON (B)(6) 2020 THAT SHE HAD EXPERIENCED MASTITIS. CUSTOMER WAS HOSPITALIZED AND PRESCRIBED THE ORAL ANTIBIOTIC, AMOXICILLIN. CUSTOMER CONTINUED PUMPING WITH HER WILLOW PUMP THROUGHOUT TREATMENT.
Patient problems: Skin Infection
MAUDE report 10619703 ↗InjuryAug 19, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED TO WILLOW CUSTOMER CARE ON 20 JUL 2020 THAT SHE EXPERIENCED A CUT ON HER NIPPLE. SHE WAS PRESCRIBED A TOPICAL CREAM. CUSTOMER CONTINUES TO PUMP AND BREASTFEED.
Patient problems: Injury; Unspecified Infection
MAUDE report 10429229 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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