Archive for the ‘Industry News’ Category
Summit Import Corporation Issues Allergy Alert on Undeclared Eggs in Bin Bin Snow Rice Cracker 5.3oz Pack and Bin Bin Rice Cracker 15.8oz Bulk Pack
FOR IMMEDIATE RELEASE – February 9, 2012 -Summit Import Corp., at 100 Summit Place, Jersey City, New Jersey, is recalling Bin Bin Snow Rice Cracker 5.3oz Pack and Bin Bin Rice Cracker 15.8oz Bulk Pack because the affected products contain egg which are not declared on the label. Consumers who are allergic to eggs may run the risk of serious or life-threatening allergic reactions if they consume this product.
The recalled Bin Bin Snow Rice Cracker, 5.3oz, UPC Code 8 852098700124 and Bin Bin Rice Cracker 15.8oz, Bulk Pack, UPC Code 8 8520098701510, both in plastic packaging, were distributed nationwide to Asian retail stores.
No illnesses have been reported to date in connection with this problem in the United States.
The recall was initiated after it was discovered the cracker products were distributed in packaging that did not reveal the presence of egg.
Consumers who are allergic to eggs and purchased Bin Bin Snow Rice Cracker 5.3oz and Bin Bin Rice Cracker 15.8oz Bulk Pack are urged to return them to the place of purchase. Consumers with questions may contact the company at 1-800-888-8228, Ext. 132, Attention: Tony Lee, Monday – Friday from 10:00AM to 5:00PM (EST).
Source: USFDA
Whole Foods Market Recalls Pumpkin Bundt Cakes For Undeclared Allergens
FOR IMMEDIATE RELEASE – February 10, 2012 – Whole Foods Market is recalling its 3 ounce and 26 ounce Pumpkin Bundt Cakes because the products contain undeclared milk. No illnesses have been reported to date, however people who have allergies to milk, run the risk of serious or life-threatening allergic reaction if they consume these products.
The recalled Pumpkin Bundt Cakes were made in Whole Foods Market store bakeries and sold at stores in Fresno, Monterey, San Rafael, San Ramon and Santa Cruz.
The 3 ounce Pumpkin Bundt Cakes were sold from a service case or displayed in small, clear plastic clamshells marked with a scale label #21630100000. Expiration dates prior to Feb. 13, 2012 are affected.
The 26 ounce pumpkin bundt cakes were sold from a service case or displayed in plastic dome containers with the scale label #21637900000. Expiration dates prior to Feb. 13, 2012 are affected.
The recall was initiated after it was discovered that the product labels did not list milk, as a sub-ingredient to cream cheese.
The necessary corrections have been made for the Pumpkin Bundt Cakes currently for sale.
Consumers who have purchased either of the affected products from Whole Foods Market may return it to the store for a full refund.
Source: USFDA
Walmart Recalls Cruller Bakery Pastries Due To Mislabeled Milk Allergen
U.S. Food and Drug Administration – February 13, 2012
Walmart recalled its eight-count packages of Cruller bakery pastries because the common name of milk was not listed following sodium caseinate, a milk derivative, on the ingredient label. People who have milk allergies that do not recognize sodium caseinate as a milk derivative run the risk of serious or life-threatening allergic reactions if they consume the product.
The eight-count packaged bakery items affected by this recall have a UPC code of 787429847 which can be found on the box label. The items affected by this recall have expiration dates of on or before Feb. 9, 2012. The pastries can be recognized as a ring-shaped twisted sweet cake similar to a doughnut. The products were labeled and sold in Walmart store bakeries in Puerto Rico and all US states with the exception of Hawaii, Maine, New Hampshire, Rhode Island and Vermont.
All stores affected by the recall have been notified to remove and discard the mislabeled products. Corrective action has been taken to ensure all current and future products are properly labeled to reflect the common name of milk as an ingredient.
One adverse reaction has been reported by a customer. Customers with questions about this recall may call the Walmart Customer Service at 1-800-Walmart (1-800-925-6278) or return the product to their nearest store for a full refund.
Source: USFDA
Nest Collective Voluntarily Recalls Select Revolution Foods Jammy Sammy – Strawberry Jam & Peanut Butter Snack Size Sandwich Bars Due to a Labeling Error (Undeclared Peanut on Inner Wrapper)
EMERYVILLE, Calif., Feb. 3, 2012 /PRNewswire/ – Nest Collective™ announced today that it is voluntarily recalling 815 cases of its Jammy Sammy™ – Strawberry Jam & Peanut Butter Flavor Snack Size Sandwich Bars due to a mislabeled inner wrapper. The cartons contain the best by date June 28, 2012 and are marked with the following universal product code (UPC) #89676600116 6 located on the bottom of the package. People who have an allergy or severe sensitivity to peanuts (or peanut butter) run the risk of serious or life-threatening allergic reaction if they consume these individual bars.
These cartons are sold online and at retail stores nationwide.
No illnesses have been reported in connection with this product and no other Revolution Foods products are affected.
The recall was undertaken because, while the cartons of this lot of product are correctly labeled, some of the individual bars are incorrectly labeled as Grammy Sammy – Honey Graham and Strawberry Yogurt™, and show the ingredient statement of that product. Both the selling unit and individually wrapped bars include information that the product was produced in a facility that processes peanuts as well as other allergens. The Jammy Sammy™ product contains organic peanut flour and organic peanut extract, but the inner wrappers are mislabeled with the Grammy Sammy information. Consumers who are allergic to peanut products should not use these products. People experiencing any health issue should seek immediate medical attention.
Source: http://www.prnewswire.com
F&S Produce Company Recalls Cobb and Spinach Salads Due to Possible Listeria Contamination
WASHINGTON, Feb. 3, 2012 – F&S Produce Company Inc., a Deerfield, N.J. establishment, is recalling approximately 389 pounds of Cobb and spinach salads. The salads contain eggs that are the subject of a Food and Drug Administration (FDA) recall due to concerns about contamination with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The following products are subject to recall:
- 10-oz. plastic containers of “Fresh Garden Highway Spinach Salad with Bacon”
- 10.75-oz plastic containers of “Fresh Garden Highway Cobb Salad”
The products subject to recall have a “Sell By” date through 2/8/2012, and bear the establishment number “Est. 39897″ as well as the USDA mark of inspection The products were distributed to a warehouse in Pennsylvania for further distribution to retail locations.
The problem was discovered when F&S Produce Company Inc . was notified by one of its suppliers that hard-cooked eggs (a product inspected by the FDA) had tested positive for Listeria monocytogenes, and are being recalled by Michael Foods Egg Products Co. The salads contain the recalled eggs and are the subject of this FSIS recall. FSIS, FDA, and the company have received no reports of illnesses associated with consumption of these products.
Source: http://www.foodsafety.gov/
California Firm Recalls Prepared Sandwiches that Contain Hard-Cooked Eggs
GH Foods CA, LLC was notified by their supplier that the eggs supplied to them were from Michael Foods, Inc, who recalled Hard-Cooked eggs due to potential contamination by Listeria monocytogenes. GH Foods CA, LLC, Sacramento, California, is therefore recalling sandwiches, associated with the affected eggs, due to potential contamination of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and individuals with weakened immune systems.
Source: http://www.foodsafety.gov/
Goodness Gardens, Inc. Recalls Chives Lot # 0201111 Because of Possible Health Risk
FOR IMMEDIATE RELEASE – May 10, 2011 – Goodness Gardens, Inc. of New Hampton, NY is voluntarily recalling Chives Lot # 0201111, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The Chives were distributed in NY, NJ, CT, MA, PA, MD, AL, IL, and VA through retail stores primarily and one wholesaler in PA.
The Chives were distributed in various plastic clamshell containers: 0.25 oz. (UPC 0 21985 20005 6), 2/3 oz. (UPC 0 21985 10004 2), in 1 lb. bags, and ½ oz. twist tie bunches.
No other Goodness Gardens Inc. products or lots are included in this recall.
The recall was the result of a routine sampling program by the Connecticut Department of Consumer Protection which revealed that the product lot contained the bacteria.
It is unlikely that any product still remains in stores but if so retailers should remove Chives Lot # 0201111 with date 5/6/11 from store shelves and inventories. Goodness Gardens, Inc. Customer Service representatives are already contacting retailers to ensure the precautionary recall is executed swiftly.
The company is not aware of any illnesses reported in connection with the recall and is coordinating closely with regulatory officials.
Consumers are urged not to consume the above lot. Consumers who purchased this item are urged to return it to the place of purchase for a full refund. Consumers with questions can contact Goodness Gardens, Inc. at 845-355-4757, Mon – Fri 9am – 4pm EDT with any questions.
Source: USFDA
Elise Grace’s Dry Food Company Issues Nationwide Allergy Alert Because Of Undeclared Allergens In Their Dry Food Products Line
FOR IMMEDIATE RELEASE – April 26, 2011 – Elsie Grace’s Dry Food Company of Frankfort, Kansas is issuing a recall of some dip mix and soup mix products because they may contain undeclared milk, soy, or wheat. People who have an allergy or severe sensitivity to milk, soy, or wheat run the risk of serious or life threatening allergic reaction if they consume these products. The complete list of these identified products is at the end of this press release.
The recalled Elsie Grace’s products were distributed in KS, NE, MO, NC, OH, IN, AR, KY, PA, OK, IL, SD, IA, WV, MI, to retail gift shops and food retailers.
Elsie Grace’s Dry Food Products are packaged as follows. Dip mixes are packed in clear, safety sealed, rectangular packs with the label stapled to it. They are not marked with any codes, UPC numbers, or dates. The ingredients are listed on the back. Dry soups are sealed in clear safety bags and then placed in a plastic lined craft paper bag. The ingredient labeling is attached to the back of the craft paper bag.
Any retailers still having any unsold products will be supplied with new corrected ingredient labels for all packages. Consumers will be able to return the product to retailers for full refund or package replacement. Replacement labeling will be identified with an asterisk (*) at the end of the ingredients.
No illnesses have been reported to date in connection with this problem.
This recall was initiated when it was discovered some of Elsie Grace’s Dry Food Products do not declare ingredients that are allergens. Subsequent investigation indicates the problem occurred in the company’s packaging process. Elsie Grace’s Dry Food Company has changed their labels to ensure customer safety.
Consumers who have purchased Elsie Grace’s Dry Food products are urged to return the product for full refund or replacement. Consumers with questions may contact the company at 1-785-292-4438 between the hours of 9am to 5pm CST Monday through Friday, or contact us at elsiegraces@yahoo.com.
Affected Products:
Elsie Grace’s Zippy Bacon Dip Mix, net weight .12-oz., and Elsie Grace’s It’s Smokin’ Dip Mix, net weight .08-oz., use imitation bacon bits which contain soy and wheat ingredients. The beef base packets in the dip mixes contain milk and soy ingredients.
Elsie Grace’s Cheesy Onion Dip Mix, net weight .08-oz., contains packets of beef base which contain milk and soy ingredients.
Elsie Grace’s Hearty Potato Soup Mix, net weight 10.6-oz., contains milk, soy, and wheat ingredients.
Elsie Grace’s Spuds and Cheese Soup Mix, net weight 10.6-oz., contains milk and soy ingredients.
Elsie Grace’s Broccoli and Cheese Soup Mix, no net weight on packages, contains milk and soy ingredients.
Elsie Grace’s White Chili Soup Mix, net weight 9.9 oz., contains milk and soy ingredients.
Source: USFDA
La Fiesta Food Products, Inc., Issues Allergy Alert due to Incorrect Ingredient Label on Dried Shredded Shrimp
FOR IMMEDIATE RELEASE – April 8, 2011 – La Fiesta Food Products, Inc., is voluntarily recalling all Dried Shredded Shrimp products due to an error on the ingredients labels. The products contain sulfites and the new labels will be updated accordingly. Certain consumers having severe sensitivity or allergies to sulfite run the risk of allergic reactions if they consume this product.
Additionally, La Fiesta Food Products, Inc., is voluntarily recalling Dried Shredded Shrimp products sold under the label Mi Pueblo.
Dried Shredded Shrimp are sold in the following packages:
|
UPC
|
Product
|
Oz
|
|
La Fiesta Brand
|
||
|
32327-00150
|
Shredded Shrimp (Camaron Molido)
|
1 7/8
|
|
32327-00181
|
Shredded Shrimp
|
3
|
|
32327-00250
|
Shredded Shrimp (Camaron Molido)
|
6
|
|
32327-00420
|
Camarón Molido (Shredded Shrimp)
|
8
|
|
Mi Pueblo Brand
|
||
|
00000-10507
|
Camaron Molido (Shredded Shrimp)
|
1 3/4
|
|
00000-10509
|
Camaron Molido
|
2 1/2
|
|
00000-10705
|
Camaron Molido
|
6 1/4
|
|
01660-07002
|
Camarón Seco Molido
|
8
|
The voluntary recall was initiated after sampling and lab analysis revealed the presence of sulfites in Dried Shredded Shrimp; the allergen warning was not printed on the labels. The new labels will state “Allergen Information: Contains Sulfites.”
No illnesses have been reported to date. As a precautionary and voluntary measure, consumers allergic to sulfites are urged to return these products to the place of purchase for a full refund.
La Fiesta Foods, Inc., has been in business since 1954. La Fiesta maintains strict quality controls on all its products. Customers can continue to expect the highest quality products from La Fiesta, as they have for the last 57 years.
Source: USFDA
B&M, Inc. Conducts Voluntary Nationwide Recall Of 6 Lot Numbers Of Archer Farms Ground Turmeric Due To Excessive Lead Levels
FOR IMMEDIATE RELEASE – April 15, 2011 – B&M, Inc. of Mount Vernon, Missouri is voluntarily recalling Archer Farms Ground Turmeric sold at Target stores in glass bottles with a net weight of 2.6 oz. (74g), due to elevated levels of lead.
Lead can accumulate in the body over time. Too much can cause health problems, including delayed mental and physical development and learning deficiencies. Pregnant women, infants and young children especially should avoid exposure to lead. People concerned about blood lead levels should contact their physician or health clinic to ask about testing.
This voluntary recall is a result of notification from B&M, Incorporated’s supplier that the Ground Turmeric they provided contained excessive levels of lead.
The Archer Farms Ground Turmeric was distributed nationwide to Target retail stores located in the following states from June, 2009, to February, 2010: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA, WA, and WI.
The product is identified at the retail store level as Archer Farms Ground Turmeric, UPC 0-85239-02612-0. The lot numbers included in this recall are 1740901A, Best By 6/23/2011; 2180902A, Best By 8/6/11; 2780906A, Best By 10/5/2011; 2920903A, Best By 10/19/11; 3060903A, Best By 11/2/2011; 0071003A, Best By1/7/2012. The lot numbers and Best By dates can be found on the bottom of the bottle.
No other Archer Farms Brand spices have been affected by this voluntary recall.
No illnesses have been reported to date in connection with this voluntary recall.
Consumers in possession of this voluntarily recalled product may return it to the store at which you purchased it. Consumers or media with questions should contact B&M, Inc. at 1-877-321-5852 (Monday – Friday, 8:30am – 4:30pm CST) or contact Target Guest Relations toll-free at (800) 316-6151.
Source: USFDA