Tuesday, June 29, 2010

Latest UPDATE Please Mass Distribute:

Inz Distributors Inc./Magic Power Coffee Inc. Date 6/28/10

2713 Coney Island Avenue

Brooklyn, NY 11235-5054



URGENT: VOLUNTARY RECALL



RE: MAGIC POWER COFFEE,

Production Dates: all dates up until 05/08/2010;

Best Before Dates: all dates up until 05/07/2012,

UPC 718122686872: 2-serving box; UPC 718122686773:

12-serving carton containing six 2-serving boxes



Recent FDA tests indicate that one of our production dates contains hydroxythiohomosildenafil, similar in structure to Sildenafil, an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making Magic Power Coffee an unapproved drug. The hydroxythiohomosildenafil drug ingredient is not listed on the product label.



Hydroxythiohomosildenafil, like Sildenafil, may interact with prescription drugs known as nitrates, including nitroglycerin, and cause dangerously low blood pressure. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.

Consequently, we are recalling the above dates from the market.



Please examine your stocks immediately to determine if you have any of the affected product on hand. If so, please discontinue distributing the affected product and promptly return via parcel post to:

ATTENTION: RETURNED GOODS

2713 Coney Island Avenue

Brooklyn, NY 11235-5054





If you have further distributed the above product, please identify your customers and immediately contact them, advise them of the recall situation, and have them return their outstanding recalled stocks to you. Return these stocks as indicated above. You will be reimbursed by check or credit memo for the returned goods and postage.



Retailers: please post this recall notice in a prominent location to alert any customers that may have purchased the product.



Please return the enclosed response form immediately providing the requested information by mail, or by fax to (718) 313-1579.



This recall is being made with the knowledge of the US Food and Drug Administration.



Customers with questions regarding this recall can contact the company at (718) 313-1579.



We appreciate your assistance in this matter.







Sincerely,



_________________

Peter R. Erlick

Vice President

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