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Swing Breast Pump 67050Recalls & reported problems

Medela AG · Powered breast pump · Class 2

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 00020451670508), received between Oct 21, 2020 and Oct 21, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Decrease in Suction” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Decrease in Suction1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 21, 2020Decrease in Suction

    ON 09/21/2020, THE CUSTOMER ALLEGED TO MEDELA CANADA THAT SHE WAS EXPERIENCING LOW SUCTION WITH HER SWING BREAST PUMP. IT WILL POWER ON BUT THERE IS NO VACUUM ACTION FROM THE MOTOR. SHE INDICATED SHE HAD MASTITIS AND NEEDED A FUNCTIONAL BREAST PUMP AS SOON AS POSSIBLE.

    Patient problems: Unspecified Infection

    MAUDE report 10711470 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.