Pump In Style 101041362Recalls & reported problems
Medela LLC · Powered Double Breast Pump · Class 2
All models of Pump In Style (5)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00020451401461), received between Mar 20, 2023 and Mar 20, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Power Problem” (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 16, 2026.
Most reported problems
Device problems
- Power Problem1
Patient problems
- Inflammation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 20, 2023Power Problem; Power Problem
ON (B)(6) 2023, THE CUSTOMER ALLEGED TO MEDELA LLC WHILE USING HER PUMP IN STYLE MAXFLOW PUMP IT WAS HAVING ISSUES STAYING POWERED ON. THE CUSTOMER ALSO ALLEGED SHE HAD MASTITIS PREVIOUSLY AND WAS PRESCRIBED ANTIBIOTICS.
Patient problems: Inflammation
MAUDE report 16574409 ↗
Other Pump, Breast, Powered devices
- Pump In Style 101041360Medela LLC · Pump, Breast, Powered127 reports
- Pump In Style Advanced PNSA Starter PumpMedela LLC · Pump, Breast, Powered82 reports
- Pump In Style 101041361Medela LLC · Pump, Breast, Powered41 reports
- Freestyle Hands-free 101044164Medela AG · Pump, Breast, Powered26 reports
- Pump in Style Advanced PNSA Starter PumpMedela LLC · Pump, Breast, Powered23 reports
- Sonata Breastpump Sonata DeluxeMedela LLC · Pump, Breast, Powered22 reports
- Pump In Style 101041265Medela LLC · Pump, Breast, Powered20 reports
- Pump Kit, Gen 3 (2S), 2PK, White, 24mm PDW48Willow Innovations, Inc. · Pump, Breast, Powered14 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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