FDA Device Intelligence
HomeHYGEIA II MEDICAL GROUP INC › Evolve Breast Pump, PAS

Evolve Breast Pump, PAS

HYGEIA II MEDICAL GROUP INC · Model 10-0152 · UDI-DI 00865278000486

HGX
10
510(k) clearances
5,563
Adverse events (2 deaths)
8
Recalls
117
Facilities

Description

A hospital grade double electric breast pump, powered by AC or battery power, used to extract milk from a mother’s breast. The milk will be collected and used to feed infants. The device permits a user to vary the suction strength, and with the use of accessory parts to collect and funnel the breast milk into storage containers. The device utilizes protective measures to prevent the build-up of excessive negative pressure

Recalls

DateFirmReason
2017-07-10AMEDA, INC.Two specific lots was incorrectly manufactured containing a UK power adapter.
2014-03-18Energizer Personal CareSome of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.
2011-01-10Medela IncThe performance of the pumps may be compromised due to the potentiometer used on the circuit board. Affected pumps may not turn on, may turn off on its own, may reduce or lose suc
2010-08-06Medela IncThe product sterility may be compromised due to possible pinholes in the rigid tray of the package.
2010-08-06Medela IncThe product sterility may be compromised due to possible pinholes in the rigid tray of the package.
2010-08-06Medela IncThe product sterility may be compromised due to possible pinholes in the rigid tray of the package.
2010-08-06Medela IncThe product sterility may be compromised due to possible pinholes in the rigid tray of the package.
2010-03-15Medela IncThe non-sterile devices were erroneously packaged with instructions stating the devices are sterile and do not require cleaning before first use.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.