YOUHA
Ningbo Youhe Mother And Baby Products Co., Ltd. · Model The INs NEXT · UDI-DI 06972798250155
1
510(k) clearances
5,556
Adverse events (2 deaths)
8
Recalls
118
Facilities
Description
The subject devices are wearable-style breast pumps designed for lactating women to express and collect milk from the breast. They are electrically powered, software controlled, digital pumps for a single user. The subject devices include The INs, The INs Gen 2, The INs NEXT, P1s, and P3 models, which are capable of expression,massage, and mixed modes with ten associated suction levels for each. All five models have a single pumping configuration and can be operated in ‘normal’ or ‘quiet’ modes.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-07-10 | AMEDA, INC. | Two specific lots was incorrectly manufactured containing a UK power adapter. |
| 2014-03-18 | Energizer Personal Care | Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock. |
| 2011-01-10 | Medela Inc | The 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 |
| 2010-08-06 | Medela Inc | The product sterility may be compromised due to possible pinholes in the rigid tray of the package. |
| 2010-08-06 | Medela Inc | The product sterility may be compromised due to possible pinholes in the rigid tray of the package. |
| 2010-08-06 | Medela Inc | The product sterility may be compromised due to possible pinholes in the rigid tray of the package. |
| 2010-08-06 | Medela Inc | The product sterility may be compromised due to possible pinholes in the rigid tray of the package. |
| 2010-03-15 | Medela Inc | The non-sterile devices were erroneously packaged with instructions stating the devices are sterile and do not require cleaning before first use. |
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Get your free API keyRead the docsData 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.