Ton Shen Health DHZC-2 Tablet Recall [US]

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US/Silver Spring: Ton Shen Health DHZC-2 Tablet Recall [US]Ton Shen Health recalls certain batch/lots of DHZC-2 Tablets due to suspected elevated Lead levels, a serious health hazard. FDA:

Direct link:

Additional information:
The US Food and Drug Administration (“FDA”) reports the following nutritional supplements are subject to this recall:

  • DHZC-2 Nutritional Supplement Tablets, sold in 1.6-ounce, white plastic packages marked with lot number 2163-844 on the bottom of the bottle and a UPC: 616042102727. The recalled Nutritional Supplements were mostly sold locally in Chicago area in retail stores. In addition, some Supplements were distributed to other US states through mail orders.

Please consult the photograph above for details of the food’s packaging, design and retail presentation.

According to the FDA, the potential for contamination was noted after FDA notice of higher level of Lead presence in DHZC-2 samples. The sale of the product has been suspended and inventory put on hold while FDA and the company continue to investigate the source of the problem. One (1) illness has been reported to date.

==> For information about Lead Poisoning, please consult the “Illnesses” tab on this site, located at the top of this page.

If you believe you have purchased or have in your possession any of the recalled nutritional supplements, please do not consume them directly nor use them as an ingredient in another dish or preparation. Instead, return the supplement to the store where you purchased it for a full refund.

If you have any questions about this recall, please contact the company at 1-312-842-2775 from 9:30 AM to 5:00 PM Central Time.

==> To see other recalls and notifications caused by suspected elevated levels of Lead contamination, please search for “lead” using the Search Box at the top of this page.

Want to read more about this recall? Please click on the links above to visit the originating site.

Want to read more about other recalls? Please click on the links below.


Additional information about this recall:
Recalls Direct RIN: 7449-2016
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