Recalls – Smoked Fish Spread, Chicago Triple Mix Popcorn and Duro Extend Capsules for Men

Wisconsin Business Recalls Smoked Fish Spread

November 30, 2010 – Rushing Waters Fisheries, Palmyra, is recalling about 225 pounds of smoked trout and smoked salmon spreads, because the products may be contaminated with Listeria monocytogenes.

No illnesses have been reported from eating this product. The contamination was discovered through routine testing conducted by the Wisconsin Department of Agriculture, Trade, and Consumer Protection.

The recalled products are smoked trout spread labeled lot number 00694 with a sell-by date of Dec 13, and smoked salmon spread labeled with lot 50012 with a sell-by date of Dec 11. Lot numbers and dates are on the bottom of the container. Affected smoked fish spreads were sold in eight-ounce containers and 4.5-pound round plastic tubs in southern Wisconsin and northern Illinois.

Consumers who have this product in their refrigerator can discard it or return it to the place of purchase for a refund. For more information contact Rushing Waters at 1-800-378-7088.

Only the smoked fish spreads with the matching lots and dates are being recalled; no other Rushing Waters Fisheries LLC products are included in the recall.

Most healthy individuals are either unaffected by Listeria or experience mild flulike symptoms. However, it can cause complications in pregnant women and have more serious effects on newborns, older adults and people with compromised immune systems.


Lobby Shoppes, Inc. Issues An Allergy Alert On Milk And Soy Products In “Cheese Popcorn, Chicago Triple Mix Popcorn And Caramel Corn”

Lobby Shoppes, Inc. of Springfield, OH, is recalling the following three (3) products from distribution: Gourmet Cheese Popcorn in 12 oz. bags UPC Code 08299 11201 and 24 oz. bags; Chicago Triple Mix Popcorn in 12 oz. bags UPC Code 08299 11203; and (Delicious) Caramel Corn in 2 ½ lb. bags, 4 lb. bags, and 9 oz. tubs UPC Code 08299 11202. All recalled products are packaged in either clear plastic bags or clear plastic tubs. These products are subject to recall because they contain undeclared ingredients, milk and soy. People who have allergies to milk and soy run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled Gourmet Cheese Popcorn, Chicago Triple Mix Popcorn and Caramel Corn were distributed in grocery stores throughout Ohio and were sold in the Lobby Shoppes, Inc. showroom in Springfield, Ohio.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the product labels did not disclose the presence of milk and soy in its contents.

Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased 12 and 24 oz. bags of Gourmet Cheese Popcorn, 12 oz. bags of Chicago Triple Mix Popcorn and 2 ½ and 4 lb. bags of Caramel Corn or 9 oz. tubs of Caramel Corn are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company Monday through Friday between the hours of 9:00 AM and 5:00 PM at 1-800-422-3992.


Intelli Health Products, Issues an Expansion to All Lots of their Voluntary Nationwide Recall of Duro Extend Capsules for Men Marketed as Dietary Supplements

December 2, 2010 – Intelli Health Products announced today that it is expanding their voluntary nationwide recall ofDuro Extend Capsules For Men, to include all lot codes.  Intelli Health Products is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that laboratory analysis of Duro Extend Capsules For Men found the product to be adulterated with Sulfoaidenafil, an analogue of Sildenafil which is an FDA approved drug used in the treatment of Erectile Dysfunction (ED), making it an unapproved new drug.

Use of this product may pose a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

Duro Extend Capsules are sold nationwide. The products are sold individually as a blister pack containing one capsule per unit, in 12-pack or 24-pack display boxes, and in bulk in 3 count and 10 count bottles.  Lot number and expiration dates appear on the seal.  Consumers who have Duro Extend Capsules in their possession should stop using them immediately.

In the event of any adverse side effects due to the consumption of these products, consumers should contact a physician immediately. Any adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.


Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: Mail to address on the pre-addressed form.

Fax: 1-800-FDA-0178

The Company is advising consumers to return any unused Duro Extend Capsules, to the retail location from which it was purchased or to the Company directly if it was purchased from the Company as a part of its Direct Response Program. Consumers can send unused capsules directly to the company.

Intelli Health Products

80 Southwest 8th Street

Suite 2000

Miami, FL 33130

Phone: 1-800-861-6022

Intelli Health Products conducts stringent quality control testing on both raw materials and finished products. Previous testing protocols did not include a test for the presence of Sulfoaidenafil but Intelli Health Products assures consumers that this deficiency is being rectified. Intelli Health Products apologizes for any inconvenience and expresses its concern for the health of consumers by conducting a voluntary recall action.  Intelli Health Products promises to ensure quality and integrity of all its products and the company is working closely with the FDA in the recall process.

Save pagePDF pageEmail pagePrint page

Leave a Comment