Tag Archives: Food

Frontier Co-op Initiates Voluntary Class 1 Recall Due to Possible Health Risk from Organic Garlic Powder

Posted on by

recall-3Frontier Co-op is voluntarily recalling several of its products manufactured with organic garlic powder that were sold under its Frontier and Simply Organic brands, and one product sold under the Whole Foods Market brand due to potential Salmonella contamination. To date, no illnesses have been associated with these products.

The product in question was raw material received by Frontier, which tested positive for Salmonella during a test by the United States Food and Drug Administration. Given that Salmonella may be present, Frontier is immediately initiating this recall.

Frontier Co-op is immediately initiating added precautions to the safety of the supply chain and instituting additional product testing, beyond FDA guidelines, to mitigate any future occurrence.

Consumption of products containing Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditic and arthritis.

Recalled products were sold in all 50 states and in some parts of Canada to distributors, retailers and consumers. Below the release is a list of products containing the organic garlic powder. Images of the affected products can be viewed at the following link: http://www.frontiercoop.com/recalldisclaimer icon.

On foil bulk packages, the four-digit lot code will be found on the front label directly above the UPC code. On bottled items, the four-digit lot code can be found on the bottom of the bottle. On seasoning mixes, the four-digit lot code is embossed on the right side of the packet.

Consumers should not consume these products and should either throw away any remaining products or return to the point of purchase for a refund.

Please contact Frontier Co-op with any questions or to inquire about replacement or reimbursement at 1- 800-669-3275 Monday through Friday from 8:00 a.m. to 5:00 p.m. Central time.
Continue reading →

Maternal Science, Inc. Issues Allergy Alert on Undeclared Milk in Healthy Mama® Boost It Up!™; Mango Drink

Posted on by

HMBoostNew5595-sq300Maternal Science, Inc. of Montvale, NJ, is voluntarily recalling healthy mama® Boost It Up!™ Drink because it contains undeclared milk (whey protein isolate). People who have an allergy to milk run the risk of serious or life-threatening allergic reaction if they consume this product. healthy mama® Boost It Up!™ Drink is manufactured for and distributed by Maternal Science, Inc. and sold nationwide through limited retailers and via internet sales. healthy mama® Boost It Up!™ Drink is packaged in a plastic bottle with a white label containing 12 fl oz per bottle (see labels below). The affected lots entered the marketplace on April, 2014. The lots affected are listed below.

Product name Package Size Lot# Date Best By UPC Code
healthy mama® Boost It Up! Mighty Mango with Ginger 12 fl oz. 14275-11 bottle 10/2015 810758020058
healthy mama® Boost It Up! Mighty Mango 12 fl oz. 14090-11 bottle 03/2015 810758020058

To date no illnesses have been reported. The recall was initiated after it was discovered during an internal review that healthy mama® Boost It Up!™ Drink containing whey protein isolate (milk) was distributed in packaging that did not reveal the presence of milk. Consumers who are allergic to milk and purchased healthy mama® Boost It Up!™ Drink are urged not to consume the product.

Consumers who purchased the affected lots of healthy mama® Boost It Up!™ Drink may return it to: ATTN: BOOST IT UP RETURN, 225 Long Ave, Hillside, NJ 07205 for a full refund or exchange. Customers may contact the company at (855) 773-4426, Monday–Thursday, 9AM – 5PM, ET or email Inquiries@healthymama.com for further instructions and claim processing.

Urgent: El Popocatepetl Ind., Inc. issues an allergy alert on Sundried Tomato, Spinach Pesto, and Chipotle Wraps

Posted on by

wraps-1

El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El Popocatepetl’s 8 in. Chipotle, Spinach Pesto, and Sun Dried Tomato Wraps because they may contain undeclared milk and Yellow #5. People who have allergies to milk and/or Yellow #5 run the risk of serious or life-threatening allergic reaction if they consume these products.

El Popocatepetl’s 8in. Flavored Wraps were distributed in the state of Illinois, primarily in the Chicago area.

The information on how the recalled products can be identified is listed below:

Product Name: 8in. Sundried Tomato
Brand Name: El Popocatepetl
Description: 8in. Tomato Flavored Wrap
UPC: 0 20784 99505 7
Any Product with the Best By Date of
April 1, 2015 and Before.
Product Name: 8in. Spinach Pest
Brand Name: El Popocatepetl
Description: 8in. Spinach Flavored Wrap
UPC: 0 20784 58314 8
Any Product with the Best By Date of
April 1, 2015 and Before.
Product Name: 8in. Chipotle
Brand Name: El Popocatepetl
Description: 8in. Chipotle Flavored Wrap
UPC: 0 20784 78248 0
Any Product with the Best By Date of
April 1, 2015 and Before.

The recall was initiated during a review of the product ingredients and the labeled ingredients revealed milk and Yellow #5 was present in an ingredient used to make the flavored wraps but not listed as ingredients on the labels. No Illnesses have been reported to date.

All recalled products are being removed from the store shelves. No other El Popocatepetl products are involved in this recall.

Consumers who have purchased the recalled product can return it to the place of purchase for a full refund. Consumers with questions may contact the Company Consumer Department at 773-843-0888.

Hummingbird Wholesale Issues Allergy Alert on Undeclared Milk in Organic Chocolate Hazelnut Butter

Posted on by

hummingbird-1WASHINGTON — Hummingbird Wholesale in Eugene Oregon is recalling 110 jars of Hummingbird Brand Organic Chocolate Hazelnut Butter that may contain undeclared milk. People who have an allergy or severe sensitivity to milk products run the risk of serious or life threatening allergic reaction if they consume this product.

No illnesses have been reported to date.

The recalled product sold to retail outlets in California, Oregon, and Washington and directly to consumers in Oregon in 1 pound (454 gram) glass jars that show lot number of 15023 on a white sticker on the jar between the dates of 1/27/15 and 2/19/15.

HW Item # Lot # UPC Code
N270 15023 6-96859-11035-1

The recall was initiated after it was discovered that a supplier had changed the ingredients without notice to include milk in the 65% dark chocolate used to make the Organic Chocolate Hazelnut Butter. The label does not show milk as an ingredient. Only lot # 15023 was made with the affected chocolate.

Consumers who purchased this product are welcome to return it to the place of purchase for a full refund, or to contact Hummingbird at 541-686-0921 ext. 105 from 8am to 4pm PST Monday through Friday.

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

Hummingbird Wholesale has taken immediate action to recall the affected Organic Chocolate Hazelnut Butter in order to ensure the safety of its consumers.

Hummingbird Wholesale is dedicated to providing the highest quality organic and raw products, and the safety of our customers is our number one priority.

ESS Food Recalls Pork Products Produced Without Benefit of Import Inspection

Posted on by

USDA-RECALL-1WASHINGTON – ESS Food, a Danish establishment, is recalling approximately 50,904 pounds of pork belly product produced in Poland that was not presented at the U.S. point of entry for inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Without the benefit of full inspection, a possibility of adverse health consequences exists.

The boneless pork belly was produced on various dates from March 3, 2014 to April 11, 2014. The following product is subject to recall:

Approximately 40-lb. boxes containing 4-5 pieces of “PINI POLONA PORK BELLY BONELESS”

The products subject to recall bear the establishment number “10023802” inside the Polish mark of inspection. The products were shipped to a distributor in Texas and a processing facility in Iowa.

The problem was discovered during routine surveillance of storage facilities when an FSIS investigator observed that the products lacked USDA import inspection marks.

This is a Class I Recall which indicates a health hazard situation where there is a reasonable probability that the use of the product will cause serious, adverse health consequences or death.

FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Consumers or Media with questions about the recall can contact Michael Stentebjerg, Area Manager, at (404) 254-8510.

California Firm Recalls Beef Products Produced Without Benefit of Import Inspection

Posted on by

chicken-1WASHINGTON – ATM International USA, Inc., a Torrance, Calif. establishment, is recalling approximately 1,999 pounds of boneless beef products that were not presented at the U.S. point of entry for inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Without the benefit of full inspection, a possibility of adverse health consequences exists.

The boneless beef products were imported from Japan on various dates between Oct. 9, 2014 – Jan. 15, 2015, and labeled in Japanese only.

  • Various weights and cuts of vacuum packed chilled boneless beef.

The vacuum packaging bears the Japanese translation for the following cuts:

  • Tender loin
  • Strip loin
  • Ribeye
  • Chuck Roll
  • Top Sirloin Butt
  • Chuck Ribs
  • Bottom Round
  • Top Round
  • Clod
  • Brisket
  • Short Plate
  • Short Rib
  • Knuckle

The above products would have been shipped either inside of a cardboard box with the Japanese establishment number “M2” and a box marking of “MZA-TN41”, “MZA-TN28” or “MZA-TN1” or inside of a Styrofoam box bearing the establishment number “EST. 27510” inside the USDA mark of inspection. These products were shipped to distributors and retail locations in Arizona, California, and Washington.

The problem was discovered during routine review of product tracking records.

FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Tuffy’s Pet Foods, Inc. Issues Voluntary Recall Nutrisca Dry Dog Food

Posted on by

ucm434026PERHAM, MN – Tuffy’s Pet Foods, Inc. of Perham, MN is voluntarily recalling specific lots of 4 lb. bags of Nutrisca Chicken and Chick Pea Recipe Dry Dog Food because they have the potential to be contaminated with Salmonella. Tuffy’s manufactured the product for Nutrisca.

The recalled product was distributed in the 4 lb. bags nationwide to distributors, brokers, retail stores, and internet retailers. The recalled product is limited to Nutrisca Chicken and Chick Pea Recipe Dry Dog Food in 4 lb. bag sizes, bearing UPC Code “8 84244 12495 7” (found on lower back of the bag). Products included in the recall are identified by the below first 5 digits of the Lot Code (found on upper back of the bag) and “Best by Dates” (found on upper back of the bag). No other bag sizes or other Nutrisca dog food, cat food, biscuits/treats, supplements or other products, are affected by this announcement.

First five digits of Lot Codes:
4G29P, 4G31P, 4H01P, 4H04P, 4H05P, 4H06P

Best By Dates:
Jul 28 16, Jul 30 16, Jul 31 16, Aug 03 16, Aug 04 16, Aug 05 16

The recall was initiated after a routine sampling program by the Ohio Department of Agriculture revealed the presence of Salmonella in one 4 lb. bag of product. The company is coordinating this voluntary recall with the FDA, and is issuing the recall action out of an abundance of caution.

Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. No Salmonella-related illnesses in people or animals have been reported to date in association with these products.

Consumers who purchased the 4 lb. bags of the dry dog food product subject to the voluntary recall (as identified above) should stop using the product, discard it in a safe manner (example, a securely covered trash receptacle), and contact Nutrisca at the number below for further information.

For consumer information or questions regarding this voluntary recall, please contact Nutrisca at 1-888-559-8833.

Pet International Inc. Recalls 6” Beef Trachea Pet Treat

Posted on by

ucm433999Pet International of Miami, Florida is recalling 1500 units of 6” Beef Trachea Pet Treat because it has the potential to be contaminated with Salmonella. Salmonella can affect animals (i.e. dogs) eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Dogs with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets (i.e. dogs) will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your dog has consumed the recalled product and has these symptoms, please contact your veterinarian.

The 6” Beef Trachea Pet Treat was distributed to retail stores in the following Cities: Conifer, and Lakewood in Colorado.

If you have this product, use gloves and put in a double bag and throw it away as soon as possible. Do not touch the product in any way, and if you do, it’s recommended you must wash your hands immediately with an antibacterial soap.

The potentially affected product will pertain to a particular lot number, and are specific to a particular size of the pouch it’s sold in. Anyone having these products should verify the following:

Brand: Buster’s Natural Pet Supply,
Lot Code: 8501450,
Size: 6” Beef Trachea/ 12 Pack Plastic Pouch,
UPC Code: 8501450

No illnesses have been reported to date. We are still warning consumers that if any of the above information is on the package you have, do not feed it to any animals at all. It may be hazardous and should be disposed of immediately.

The recall was as the result of a routine sampling program by the Colorado Department of Agriculture and analyzed by FDA, obtained from Buster’s Natural Pet Supply in Conifer, CO. and found to be positive for Salmonella. The product sampled had a Buster’s Label on it, but was manufactured by Pet International. Buster’s Natural Pet Supply recalled the entire product from the two stores that the distributor sells it. The Pet International Inc. continues their investigation as to what caused the problem.

Consumers who have purchased 6” Beef Trachea with Buster’s Natural Pet Supply Label on it and are wishing to be refunded because of the recall, can take the product back to where bought it from, with receipt. A special form will be provided to be filled out as well. Both the form and the receipt are needed for the refund.

Consumers with any questions about the recall product may contact the company at by phone at (305) 591-3338 Monday through Friday 9:00am too 5:00pm EST or via e-mail at sergioh@petint.com.

Detox Transforms Health and Nutrition Issues Voluntary Nationwide Recall of Dietary Supplements

Posted on by

dextrol-recallDetox Transforms Health and Nutrition, Garner, NC announced it is conducting a voluntary recall of the following dietary supplements, to the consumer level, because they contain undeclared drug ingredients making them unapproved drugs.

Product Name Bottle Color Label # Capsules UPC Lot Expiration
EDGE Amplified Weight Release White Purple label 60 852175004174 ALL
iNDiGO White Dark blue label 60 852175004044 000034 4/10/2017
AMPD Gold Bee Pollen White Black label 60 852175004181 ALL
BtRim Max White Dark Red label 60 852175004068 00002 4/27/2017
iNSANE Bee Pollen White Bright Red label 60 852175004082 0000:02 6/20/2017

FDA analysis found iNDiGO and BtRim Max to contain undeclared phenolphthalein. The health risks of phenolphthalein could include potentially serious gastrointestinal disturbances, irregular heartbeat, and cancer with long-term use. FDA analysis found EDGE Amplified Weight Release and iNSANE Bee Pollen to contain undeclared phenolphthalein and fluoxetine. In addition to the potential adverse health consequences for phenolphthalein, the concomitant use of fluoxetine with other medications such as MAO-Inhibitors and serotonin precursors (such as tryptophans) is either contraindicated or is not recommended. Fluoxetine is an SSRI with potentially life-threatening side effects that is given to patients to treat depression, anxiety, panic attacks, obsessive-compulsive disorder, or bulimia. Even when taken as prescribed, fluoxetine has been associated with serious side effects including suicidal thinking, abnormal bleeding, and seizures. Thus, any adverse reaction that is possible with fluoxetine is possible with the fluoxetine-containing dietary supplement product. In patients on other medications for common conditions (aspirin, ibuprofen, or other drugs for depression, anxiety, bipolar illness, blood clots, chemotherapy, heart conditions, and psychosis), ventricular arrhythmia or sudden death can occur with concomitant use of fluoxetine. FDA analysis found AMPD Gold Bee Pollen to contain undeclared sildenafil which has the potential to interact with medications. Males taking nitrates are at risk for life threatening hypotensive events. Certain medications such as ritonavir, ketoconazole, and itraconazole as well as consuming substantial amounts of alcohol can increase the effects of sildenafil.

The products were distributed nationwide via the internet and retail stores. No illnesses have been reported to date with the use of these products.

Detox Transforms has ceased distribution of the products as the company is working in close cooperation with the U.S. Food and Drug Administration (FDA) to fully resolve this issue. Detox Transforms is notifying its distributors and customers by email, telephone, and mail and is arranging for return of all recalled products. Consumers/distributors/retailers that have these products which are being recalled should stop use and return to place of purchase for a full refund.

Consumers with questions regarding this recall may contact Detox Transforms at 877-404-7873 or 919-341-9050 between the hours of 10am – 6pm (EST), Monday through Friday. 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 these of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

See’s Candies, Inc. Issues alert on Red Heart with Assorted Chocolates

Posted on by

ucm433410SAN FRANCISCO — See’s Company of San Francisco is recalling all 8 oz Classic Red Hearts with Assorted Chocolates with bar code 737666091201 and stamped date L.A.N. 048/15 because it contains undeclared tree nuts. People who have an allergy or severe sensitivity to tree nuts (e.g.: almonds, walnuts, pecans, coconut) run the risk of serious or life-threatening allergic reaction if they consume these products.

Product was distributed nationwide through See’s Candies Retail Stores and Mail Order (Web/Phone/Catalog). The product is sold packaged at the stores in 8oz Red Heart boxes. No illnesses have been reported to date. The product UPC is: 737666091201.ucm433411

The recall was initiated after a retail store discovered a red heart with the incorrectly labeled base mixed in with properly labeled bases.

Consumers who have purchased Sees’ Candies Classic Red Hearts with Assorted Chocolates with bar code 737666091201 and lot L.A.N.048/15 and are sensitive to tree nuts are urged to return the hearts to the place of purchase for a full refund or exchange. Consumers with questions may contact the company at 1-800-789-7337 (Monday thru Friday, 8:30am to 4:30pm PDT).