LA County Public Health - Environmental Health

Welcome to the Food Recall webpage. This page is maintained by the Environmental Health Division of the Los Angeles County Department of Public Health in order to provide consumers with the latest information about food recalls affecting the County. In addition to posting details about recalls on this page, Environmental Health actively follows up on reports of adulterated food, auditing retailers to ensure that all contaminated products have been removed from store's shelves. Please bookmark this page or follow us on twitter at LAPublicHealth for frequent updates.
Consumers who have any of these products in their possession should return the product to the place of purchase or see full press release for details for disposition.

If you believe that you became sick from eating or drinking something, you can file a report by clicking this link Food Illness, or by calling 1-888-397-3993.

May 13, 2013

California Firm Recalls Pork Pie Products Due to Misbranding and Undeclared Allergens

Congressional and Public Affairs
Joan Lindenberger
(202) 720-9113

WASHINGTON, May 10, 2013 - Jolly Good Meat Products, a Los Angeles, Calif. establishment, is recalling approximately 1,471 pounds of pork meat pie products because of misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products contain milk, a known allergen which is not declared on the product label.

The following products are subject to recall:

7-oz. packages of “Jolly Good Melton Mowbray Brand Pie” bearing the establishment number “Est. 6216” inside the USDA mark of inspection. The packages contain two pork pies. The products were produced on various dates from Nov. 8, 2012 through April 24, 2013.

The products were distributed to restaurants and distributors in California.

The problem was discovered by FSIS during a routine label review. Milk is a subingredient of margarine used in the product. While margarine is listed as an ingredient in the product package, milk is not listed. FSIS and the company have received no reports of adverse reactions associated with consumption of these products. Anyone concerned about an adverse reaction should see a health care professional.

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Last Modified: May 13, 2013

Retail Distribution List (PDF Only)

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May 13, 2013

Smart & Final Expands Recall to Include Additional Production Dates Allergy Alert - Undeclared Wheat, Milk and Eggs in La Romanella Tri-Color Cheese Tortellini

Contact:
Consumer:
(800) 894-0511

FOR IMMEDIATE RELEASE - May 10, 2013 - Smart & Final of Los Angeles, Calif., which previously announced a recall of certain production dates of 2.5 lb - La Romanella Tri-Color Cheese Tortellini, is expanding its recall to include additional production dates due to undeclared wheat, eggs and milk. People who have an allergy or severe sensitivity to wheat, eggs and /or milk run the risk of serious or life-threatening allergic reaction if they consume these products. The expanded recall is in addition to products recalled on April 25, 2013.

The product is in a 2.5 pound plastic bag, additional lot codes: 062612, 071712, 91412, 100212, 101312, 101512, 101612, 111912, 120112, 120312, 010813, 011813, 012813. Previous recalled lot codes: 020713, 022513, 031113, 031813, 031913 and 040313. The UPC number is 728920130026.

Product was distributed to California, Arizona, Oregon, Washington, Idaho and Nevada and sold through Smart & Final stores or Cash & Carry stores.

No reports of injury or illness have been received to date.

This recall was initiated after it was discovered that the label failed to contain an ingredient statement.

Consumers who have purchased this product may return the product to the store where it was purchased for a replacement or a refund. Consumers with questions may contact Smart & Final's consumer relations at (800) 894-0511, Monday through Friday, or visit our website at: www.smartandfinal.com/products/productrecalls.aspx.

Initial Press Release

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May 10, 2013

Pure Herbs Ltd. Issues Allergy Recall Alert on Undeclared Allergens (Milk and Soy) in Protein Extract Urgent Undeclared Allergen Labeling Recall In Pure Herbs Ltd. Protein Extract

Contact:
Consumer:
586-446-8200

FOR IMMEDIATE RELEASE - May 6, 2013 - Today, Pure Herbs Ltd., Sterling Heights, MI is voluntarily recalling the 4oz and 1oz bottles of Protein Extract because they contain undeclared allergens - milk and soy. This labeling error was discovered during a routine Food and Drug Administration (FDA) inspection when a review of the ingredients found that milk and soy allergen ingredients were not listed on our main label. People who have an allergy or severe sensitivity to milk or soy run the risk of serious or life-threatening allergic reaction if they consume this product. There have been no illnesses reported to date in connection with this product. This product is a food safety concern only for people who are allergic to milk or soy. Customers with an allergy or sensitivity to milk or soy should not consume this product.

This product has been shipped to distributors nationwide. The product reached consumers through mail orders, direct delivery or retail stores.

The Protein extract product recalled was distributed prior to April 30, 2013. There are no expiration dates on the Protein extract. The Protein extract is packaged in 4oz and 1oz amber glass bottles with a Pure Herbs Ltd. Logo, Natural Herbal Extracts underneath the logo, and the name Protein on the front panel. This voluntary recall is limited to the Protein Extract packaged in 4oz and 1oz amber glass bottles. All lot numbers are included. Lot numbers 243 and 050812, represent batch 101310 which was manufactured on October 13, 2010 and was distributed from February 2012 to February 2013. Lot number 012712A was manufactured on January 27, 2012 and was distributed from March 2013 to April 2013. The lot numbers are printed on the bottom of the front panel to the right. No other Pure Herbs, Ltd. products are impacted.

Pure Herbs, Ltd. will work with Distributors to ensure that the recalled products are removed from their shelves. We ask that any un-used product be returned to be re-labeled. New labels have been printed that do declare these allergens and the product is currently being labeled utilizing this new label beginning May 3, 2013. In the event that consumers who are allergic to milk or soy have purchased the impacted product, they may return it to Pure Herbs for a full refund. Consumers who wish to return the product or have questions about this issue may call (586)446-8200 between the hours of 9:00 a.m. to 5:30 p.m. EST to speak with Dana Smith or Barb Jacobs, Monday thru Fri.

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May 10, 2013

Dairy Fresh Conducts Voluntary Recall of IGA® Brand “Vanilla & Chocolate” 1.75 Quart Ice Cream Because Package May Contain Undeclared Allergens (Almonds, Coconut, Soy)

Contact:
Consumer:
1-800-587-2259

Media
Jamaison Schuler
(214) 721-7766

FOR IMMEDIATE RELEASE - May 9, 2013 - Dairy Fresh is voluntarily recalling a specific batch of IGA Brand “Vanilla & Chocolate” Ice Cream (1.75 quart, 1.66L) with the plant code “3783” and a SELL BY date of 08-13-13 because it incorrectly contains Heavenly Hash ice cream, which contains almonds, coconut, and soy, which are allergens not declared on the carton. People who have an allergy or severe sensitivity to almonds, coconut, or soy run the risk of serious or life-threatening allergic reaction if they consume this product. The company is aware of one consumer who experienced an allergic reaction after consuming the product manufactured with the “SELL BY” date of 08-13-13. The company is not aware of any other complaint or illness to date related to this issue.

In an abundance of caution, the company is also recalling Vanilla & Chocolate ice cream dated between 06-08-13 and 08-27-13. The specific dates are listed below.

A small number of Vanilla & Chocolate packages were inadvertently used when the company was producing Heavenly Hash ice cream. As a result, a consumer may purchase a Vanilla & Chocolate package that contains Heavenly Hash ice cream.

This product is produced by the Dairy Fresh processing facility in Winston Salem, North Carolina, and is sold at IGA stores.

Size	Name	Flavor	UPC #	Dates	Plant code
1.75 quart(1.66L)	IGA Brand	Vanilla & Chocolate	4127046131	Sell by: 06-08-13 07-19-13 08-02-13 08-13-13 08-27-13	3783

This product is produced by the Dairy Fresh processing facility in Winston Salem, North Carolina, and is sold at IGA stores.other Vanilla & Chocolate dated between 06-08-13 and 08-27-13. All Vanilla & Chocolate cartons carry the above referenced Universal Product Code (UPC) and plant code “3783.”

Consumers who purchased the product may discard it and return the product package to the place of purchase for a full refund or exchange. Consumers with questions can contact Dairy Fresh 1-800-587-2259 between 8:00 AM to 5:00 PM, Central Time, Monday through Friday, excluding holidays.

The U.S. Food and Drug Administration has been notified of this voluntary recall.

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May 8, 2013

Beamonstar Products Issues Voluntary Nationwide Recall of SexVoltz, Velextra, & Amerect Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients

Contact:
Consumer:
480-735-1424

Media
Jeff Bolanos
480-522-0566

FOR IMMEDIATE RELEASE - May 7, 2013 - Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU’s 626570609490, 827912089028, 626570617877, 626570615316, Velextra brand SKU’s 626570613855, 626570619055, 626570617860, 626570617563, Amerect SKU’s 626570619031, 626570619598 capsules to the retail level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. Amerect is voluntarily recalled because it has the potential to contain undeclared tadalafil. Tadalafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the products unapproved new drugs.

Risk Statement: These undeclared active ingredients poses a threat to consumers because tadalafil 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. BeaMonstar Products has not received any reports of adverse events to date related to this recall.

The product is used as a sexual enhancement product and all 3 products are packaged in blister type packaging in 1 & 2 caps, and in 4 capsule and 10 capsule bottles. The affected SexVoltz brand SKU’s are 626570609490, 827912089028, 626570617877, 626570615316. The affected Velextra brand SKU’s 626570613855, 626570619055, 626570617860, 626570617563. Amerect SKU’s are 626570619031, 626570619598. The affected ‘Maximum Strength’ SexVoltz, Velextra, and Amerect are all lots distributed and sold from January of 2012 to May 7, 2013 and contain various expiration dates. SexVoltz, Velextra, and Amerect was distributed Nationwide to wholesalers, retail, and via internet.

BeaMonstar Products is notifying its distributors and customers by email and telephonically and is arranging for credit of all recalled products. Consumers/distributors/retailers that have Sexvoltz, Velextra or Amerect which is being recalled should return to place of purchase.

Consumers with questions regarding this recall can contact BeaMonstar Products by 480-735-1424 or info@beamonstar.com Mon-Friday from 8am-1pm (MST). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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.

Online:www.fda.gov/medwatch/report.htm
Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm
Mail to address on the pre-addressed form.
Fax: 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

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May 8, 2013

California Firm Recalls Ready-To-Eat Smoked Pork Sausage Products Produced Without the Benefit of Inspection

Congressional and Public Affairs
Elizabeth Boody
(202) 720-9113

WASHINGTON, May 7, 2013 - Tibor’s Gourmet, a Palmdale, Calif., establishment, is recalling approximately 200 pounds of ready-to-eat smoked pork sausage products because they were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The following Tibor’s Gourmet products are subject to recall: [Labels (PDF Only)]

“Ready To Eat” Gourmet Hungarian Brand Mild Smoked Sausage
"Ready To Eat” Gourmet Hungarian Brand Spicy Smoked Sausage

Each package bears the establishment number "EST. 44866" inside the USDA mark of inspection. The products were produced between Feb. 25, 2013, and May 2, 2013, and shipped to a retail chain in Los Angeles and Orange counties.

The problem was discovered by an FSIS investigation, during which the product was found in a retail location. The company was in the process of obtaining federal inspection, but had not received a Grant of Inspection.

FSIS has received no reports of illness due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

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Last Modified: May 7, 2013

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May 7, 2013

Chang Kwung Issues A Voluntary Nationwide Recall of Lightning Rod Capsules Due to Undeclared Ingredient

Contact:
Consumer:
Ralph Ceglia
747-444-1843
rxxxone777@gmail.com

FOR IMMEDIATE RELEASE - May 7, 2013 - Chang Kwung announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplements sold under the brand name Lightning Rod 500 mg per capsule packaged in 3-count, UPC 6 89076 20257 2 and 12-count bottles, UPC 6 89076 20297 8.

Chang Kwung is conducting a voluntary recall after being notified by the US FDA that analytical testing found the Lightning Rod Capsules to contain an analogue of Sildenafil. Sildenafil is the active ingredient in an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making Lightning Rod Capsules an unapproved new drug. The active drug ingredient is not listed on the label for this product. 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. To date, the firm has not received any reports of adverse events related to this recall or is aware of any illnesses associated with this product.

Lightning Rod capsules are sold over the counter as a dietary supplement marketed for male sexual enhancement. It is sold nationwide via internet in 3 capsule count and 12 capsule count bottles between August 2012 and May 3, 2013.

Chang Kwung Inc. advises any customer in possession of Lightning Rod Capsules matching the description above, return any unused product, for a full refund, to the company directly. Consumers with questions regarding this recall can call 747-444-1843, Monday through Friday 9:00 AM to 5:00 PM PST, for instructions on the return and refund process. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

Chang Kwung is committed to improving its products and avoiding future recall issues by sourcing higher quality raw ingredients and expanding testing. Chang Kwung promises its customers the highest possible quality and welcomes the recall process as further evidence of our commitment to our brands, products and consumers.

Any adverse reactions or quality problems experienced with the use of these products may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Online: http://www.fda.gov/MedWatch/report.htm
Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: http://www.fda.gov/MedWatch/getforms.htm.
Mail to address on the pre-addressed form.
Fax: 1-800-FDA-0178

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May 3, 2013

Wisconsin Firm Recalls Frozen Pizzas Due To Possible Foreign Matter Contamination

Congressional and Public Affairs
Leo O'Drudy
(202) 720-9113

WASHINGTON, April 10, 2013 -Nestlé Pizza Company, a Little Chute, WI establishment, is recalling an undetermined amount of frozen pizzas that may be contaminated with extraneous materials and are the subject of a recall administered by the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) and the Food and Drug Administration (FDA), FSIS announced today.

The following products are subject to USDA recall: [Label]

California Pizza Kitchen© Limited Edition Grilled Chicken with Cabernet Sauce, UPC 71921 00781; production code is 3059525952.

Each product package above has an establishment number of P-5754. In addition, the following products are subject to FDA recall:

California Pizza Kitchen (CPK) Crispy Thin Crust White©, UPC 71921 98745; production codes are 3062525951, 3062525952 and 3063525951.

The problem was discovered after the firm received consumer complaints that small fragments of plastic were found in the CPK Crispy Thin Crust White Pizza. The problem was related to the lot of spinach used in the production of three additional varieties of pizza subject to recall. There has been one consumer report of injury thus far (a chipped tooth) associated with consumption of these products. The fragments are of clear, brittle plastic, in irregular triangles, and may have sharp edges.

All the pizzas being recalled were produced between February 26 and March 9 of this year and shipped to retail establishments nationwide.

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Last Modified: May 3, 2013

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May 2, 2013

American Lifestyle Issues a Worldwide Voluntary Recall of Vicerex Capsules and Black Ant Capsules, Marketed as a Dietary Supplement, Due to Undeclared Active Ingredients

Contact:
Consumer:
American Lifestyle
585-586-1878

FOR IMMEDIATE RELEASE - May 1, 2013 - American Lifestyle is announcing that it is conducting a voluntary recall of all lots of Vicerex UPC 893490820087 and Black Ant UPC 4026666142546. Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

Risk Statement: These undeclared active ingredients poses a threat to consumers because tadalafil and sildenafil 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. No Adverse events have been reported related to this recall.

Vicerex is sold in blister packs containing ten (10) capsules and Black Ant is sold in a box containing four (4) individually wrapped capsules. The product is distributed worldwide by American Lifestyle by on-line sales and retail. The products are being promoted for increasing desire and sexual performance. The products are sold without medical prescription.

American Lifestyle is notifying its customers by telephone and email and is arranging for return of all recalled products. Consumers who have purchased Vicerex or Black Ant capsules are urged to immediately discontinue their use and return the product to their place of purchase or directly to American Lifestyle, 640 Kreag Road, Pittsford, NY 14534. Consumers are asked to have order number or proof of purchase.

Consumers with questions regarding this recall may contact American Lifestyle at 585-586-1878 Monday through Friday 7 am to 3 pm EST.

Consumers who have purchased any of these products and have any of the mentioned medical illnesses should consult their health care providers.

Adverse reaction or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program online, by regular mail, or by fax.

Online: http://www.fda.gov/MedWatch/report.htm.
Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at http://www.fda.gov/MedWatch/getforms.htm.
Mail to address on the pre-addressed form.
Fax: 1-800-FDA-0178.

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