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The Food and Drug Administration (FDA) warns the general public against the purchase and use of the unregistered health related device:

  1. Megafresh® Compact Alkaline Water Filtration Systems

The FDA verified through post-marketing surveillance that the abovementioned health related device is not registered and the Certificate of Health Related Device Registration (CHRDR) has not yet been issued. Pursuant to the Republic Act No. 9711, otherwise known as the “Food and Drug Administration Act of 2009”, the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promotion, advertising or sponsorship of health products without the proper authorization is prohibited.

Since this unregistered health related device has not gone through evaluation process of the FDA, the agency cannot assure its quality and safety. Health related device products especially water purification device/ system shall not bear any false, deceptive and misleading claims and promotional ploys on alkaline water, oxygenated water or ionized water.

In light of the foregoing, the public is advised not to purchase the violative product in the market.

All concerned establishments are warned not to distribute, advertise, or sell the said violative health related device until CHRDR is issued, otherwise, regulatory actions and sanctions shall be strictly pursued.

All FDA Regional Field Offices and Regulatory Enforcement Units in coordination with law enforcement agencies and Local Government Units are requested to ensure that this product is not sold or made available in the market or areas of jurisdiction.

The Bureau of Customs is urged to restrain the entry of this unregistered product.

For more information and inquiries, kindly contact the FDA Center for Device Regulation, Radiation Health and Research through e-mail at, or call (02) 857-1900 loc. 8301.

To report any sale or distribution of unregistered health related device, the online reporting facility, eReport can be accessed at

Dissemination of this advisory to all concerned is hereby requested.

Attachment-> : FDA Advisory No. 2019-245