GROUND BEEF RECALL: PLEASE SHARE
RECALL ALERT: Venolin HFA Inhaler – If You or Someone You Know Uses This PLEASE Share
February 5, 2018 by
It’s Almost The 4th Of July – You MUST Read This RECALL on Fireworks – Injuries Reported
June 29, 2017 by
The Consumer Product Safety Commission has issued a recalled for fireworks just before the Fourth of July holiday weekend because of burn and injury hazards caused by unexpected explosions.
According to the recall alert, the TNT Red, White & Blue Smoke fireworks were sold at Walmart, Target, Meijer, Kroger and Albertsons stores in Ohio, Illinois Wisconsin and Vermont from May through June 2017.
There have already been three reports of burn injuries related to the product.
The recalled fireworks are pyrotechnic devices, CPSC says that make smoke when lit. They were sold in a bag containing three canisters: one red, one blue and one white. Each colored smoke firework is a cardboard cylinder tube that measures about 1 inch in diameter and 5 inches long.
The TNT logo, “Red, White & Blue Smoke” and UPC number 027736036561 appear on the packaging.
If you have purchased these items, you shouldn’t use them. Contact American Promotional Events at 800-243-1189 for a full refund. Their call center is open from 8 a.m. to 5 p.m. (CT) Monday through Friday.
You can also reach them by email at info@tntfireworks.com or online at www.tntfireworks.comand click on Product Recall at the bottom right-hand corner of the page.
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RECALL ALERT~ 600,000 Ventolin Rescue Inhalers This is a CLASS II Recall Meaning It Could Cause a Temporary Health Crisis! Please Read & Share This Information!
April 6, 2017 by
OH NO You could have a SERIOUS Problem with your Ventolin Rescue Inhaler!
This is a NEW RECALL The Recall Initiation Date is 3/22/2017.
This Recall is on Ventiolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, net weight 18 g inhalers, RX only.
Reason for Recall:
Defective Delivery System: Elevated number of units with out of specification results for leak rate.
D-0626-2017
Code Information:
Lot #: 6ZP9848, Exp 03/18; 6ZP0003, 6ZP9944, Exp 04/18.
Classification:
Class II
If patients have questions regarding a Ventolin HFA unit, or wish to know if their inhaler is included in the recall, they may contact GSK’s Customer Service Center at 1-888-825-5249, Monday-Friday, 8:30 am – 5:30 pm ET. If a patient believes his or her Ventolin HFA inhaler is not effective at relieving his or her symptoms, the patient should seek immediate medical attention from his or her healthcare provider.
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RECALL ALERT: RUN and Check Your Boxes of Taquitos – Contaminated with Extraneous Materials
March 30, 2017 by
Ajinomoto Windsor, Inc., a Lampasas, Texas establishment, is recalling approximately 35,168 pounds of frozen ready-to-eat beef taquito products that may be contaminated with extraneous materials, specifically rubber with plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen ready-to-eat beef taquito items were produced on December 30, 2016. The following products are subject to recall:
- 60-oz. plastic bags inside of a corrugated carton labeled as “JOSÉ OLÉ TAQUITOS BEEF CARNE DE RES IN CORN TORTILLAS Crispy and Crunchy,” with case codes 3366365A, 3366365B, 3366365C, 3366365D and a Best By date of December 30, 2017.
The products subject to recall bear establishment number “Est. M-5590” inside the USDA mark of inspection. These items were shipped to retail locations in California, Florida, Illinois, Missouri, New York, Ohio, Pennsylvania, Texas, and Wyoming.
The problem was discovered when Ajinomoto Windsor, Inc. received two consumer complaints of foreign material in its ready-to-eat beef products on March 14, 2017 and March 21, 2017. The foreign materials were pieces of rubber with white plastic that originated from the establishments processing equipment.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Consumers and media with questions about the recall can contact Paul Taylor, General Counsel, at (909) 477-4800.
Consumers with food safety questions can “Ask Karen,” the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from 10 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
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RECALL – We Have a HUGE Candy Recall – RUN and Check Yours
January 10, 2017 by
Palmer Candy Company Announces Voluntary Limited Recall of Select Candy Products
Recall initiated after discovery of issue with supplied ingredient
Sioux City, IOWA, (January 9, 2017) – Palmer Candy Company (www.palmercandy.com), a privately-held, fifth-generation manufacturer of chocolate and holiday confections, announced today a limited recall of certain chocolate products after being informed by a supplier that a milk powder ingredient used in a compound chocolate coating that they supply to Palmer Candy Company has the potential to be contaminated with Salmonella. The voluntary recall, in cooperation with the U.S. Food and Drug Administration (FDA) includes selected products produced between October 20, 2016 and December 9, 2016 and shipped by Palmer Candy Company to grocery, convenience store and wholesale customers nationwide.
Recalled products include the following:
UPC #s are usually on the back of the bag or bottom of containers.
Product photos are attached.
To date, there have been no reported illnesses associated with any of the products affected by this recall. Salmonella is an organism which 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 (which may be bloody), 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 (i.e., infected aneurysms), endocarditis and arthritis.
The recall is the result of a potentially contaminated milk powder ingredient recalled by Valley Milk Products, a derivative of which was included as a small portion of the ingredients by another company in a confectionary coating supplied to Palmer Candy Company. Affected products include a variety of candy products sold to retailers under the Palmer Candy Company brand, private label chocolates for retail distribution and bulk products provided to retailers for repackaging. Although testing has shown no pathogenic bacteria in the milk confectionary coatings, the company decided out of an abundance of caution to recall all products produced using any amount of the now recalled ingredients.
Marty Palmer, president and chief executive officer of Palmer Candy Company said, “We are truly sorry for any distress this recall causes to our retail customers and to consumers. We remain committed to the highest standards in food quality and safety. We are taking this recall very seriously and truly appreciate the cooperation of our customers as we work to resolve this matter promptly.”
Consumers should throw out or return these products to the point of sale for a full refund.
For more information, consumers may call to speak with a Customer Service Representative at Palmer Candy Company between 9:00 a.m. and 4:30 p.m. Central Standard Time at 712-258-5543.
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RECALL: Tyson Chicken – Check Your Packages Then Share With Friends
October 17, 2016 by
Tyson Foods, a New Holland, Pa. establishment, is recalling approximately 1,148 pounds of frozen popcorn chicken products that may be contaminated with extraneous materials, specifically hard plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
The frozen, ready-to-eat, whole grain popcorn chicken items were produced on August 10, 2016. The following products are subject to recall:
- 35 cases of 32.79-lb. “TYSON FULLY COOKED, WHOLE GRAIN GOLDEN CRISPY POPCORN CHICKEN, CHICKEN PATTIE FRITTERS” with a case code of “70368/928” on the upper right hand side of the label.
The products subject to recall bear establishment number “P-1325” inside the USDA mark of inspection. These items were shipped to a wholesale distributor in Illinois and further distributed to schools and food services in Missouri and Illinois.
The problem was discovered when the establishment received a consumer complaint from a school regarding foreign material, specifically hard plastic, found inside a bag of Tyson brand whole grain popcorn chicken product.
There have been no confirmed reports of injury or illness due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
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RECALL – Read About This Recall on Lunchables – Share With Friends
October 9, 2016 by
Kraft Heinz Company, a Fullerton, Calif. establishment, is recalling approximately 959 pounds of ready-to-eat “Lunchables Ham and American Cracker Stackers” packaged lunch products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains wheat and soy, known allergens, which are not declared on the product label.
The ready-to-eat meat and cheese packaged lunch items were produced on September 21, 2016. The following products are subject to recall:
- 3.4-oz. boxes containing four-compartment plastic trays of “Lunchables Ham and American Cracker Stackers,” with a “USE BY” date of 25 DEC 2016 and production times ranging from 9:13 to 10:00 stamped on the side of the plastic container.
The products subject to recall bear establishment number “EST. 537K” inside the USDA mark of inspection. These items were shipped to retail locations in Utah and California.
The problem was discovered on October 6, 2016, when the firm received a consumer complaint. There were no illnesses associated with the complaint.
The establishment determined that the “Lunchables Ham and American Cracker Stackers” products were incorrectly labeled with the back label for a “Nacho Lunchable” product. The back label contains the product ingredient statements and as such, the “Lunchables Ham and American Cracker Stackers” products that were mislabeled do not declare wheat and soy on the label.
There have been no confirmed reports of adverse reactions due to consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider.
Consumers who have purchased this product are urged not to consume it. This product should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.
Consumers with questions about the recall can contact the Kraft Heinz Consumer Relations Center, at 1-800-573-3877. Members of the media with questions about the recall can contact Lynne Gaila, Corporate Affairs Director, Kraft Heinz Company, at (847) 646-4396 or lynne.galia@kraftheinzcompany.com.
Consumers with food safety questions can “Ask Karen,” the FSIS virtual representative available 24 hours a day at AskKaren.gov or via smartphone at m.askkaren.gov. The toll-free USDA Meat and Poultry Hotline 1-888-MPHotline (1-888-674-6854) is available in English and Spanish and can be reached from 10 a.m. to 4 p.m. (Eastern Time) Monday through Friday. Recorded food safety messages are available 24 hours a day. The online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at: http://www.fsis.usda.gov/reportproblem.
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RUN and Check Your Cabinets For These Baby Products Voluntarily Recalled By CVS
October 9, 2016 by
CVS Pharmacy announced 9/30 that it has voluntarily withdrawn all brands of homeopathic teething products sold in its retail stores and online at CVS.com. The voluntary withdrawal is being conducted in light of the FDA’s announcement today recommending that consumers stop using these products.
The products affected by this action are:
- Baby Orajel Naturals Gel for Teething Pain, .33 oz
- Baby Orajel Naturals Gel for Teething Pain Nighttime Formula, .33 oz
- Baby Orajel Naturals Tablets for Teething Pain, 125 Count
- CVS Homeopathic Infant’s Teething Tablet, 135 Count
- CVS Homeopathic Infants’ Teething Liquid, .85 oz
- Hyland’s Baby Nighttime Teething Tablets, 135 Count
- Hyland’s Baby Teething Gel, .5 oz
- Hyland’s Baby Teething Tablets, 13 Count
- Hyland’s Baby Teething Tablets, 135 Count
- Hyland’s Teething Gel, .33 oz
CVS Pharmacy is in the process of removing these products. A “do not sell” block has been placed in the Company’s store register system to prevent further sale of any affected items.
General information about CVS Pharmacy and CVS Health is available at www.cvshealth.com.
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RECALL: Bar S – RUN & Check The Dates on Your Bar S Franks & Corn Dogs
July 20, 2016 by
The Altus, OK-based Bar-S Foods Company, late Tuesday recalled approximately 372,684 pounds of chicken and pork hot dog and corn dog products that may be adulterated with Listeria monocytogenes, according to the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS).
The ready-to-eat, chicken and pork hot dog and corn dog items were produced on July 10, 11, 12, and 13, 2016. The following products are subject to recall:
- 16-oz/1-lb. packages of “BAR-S Classic BUN LENGTH Franks MADE WITH CHICKEN, PORK ADDED” with “Use By” date of 10/11/2016 and case code 209.
- 12-oz. packages of “BAR-S CLASSIC Franks MADE WITH CHICKEN, PORK ADDED” with package code 6338, “Use By” date of 10/10/2016 and case code 6405.
- 24-oz./1.5-lb. cartons of “SIGNATURE Pick 5 CORNDOGS – 8 Honey Batter Dipped Franks On A Stick” with a “Use By” date of 4/6/2017 and case code 6071.
- 42.72-oz./2.67-lb. cartons of “BAR-S CLASSIC CORN DOGS – 16 Honey Batter Dipped Franks On A Stick” with “Use By” dates of 4/7/2017 and 4/8/2017 and case code 6396.
- 48-oz./3-lb. cartons of “BAR-S CLASSIC CORN DOGS – 16 Honey Batter Dipped Franks On A Stick” with package code 14054, “Use By” dates of 4/6/2017 and 4/9/2017, and case code 14038.
The products subject to recall bear establishment number “EST. P-81A” inside the USDA mark of inspection. These items were shipped to retail locations nationwide.
Bar-S Foods notified FSIS’ Dallas District Office earlier on July 19, 2016, of its intention to recall five chicken and pork hot dog and corn dog products that could potentially be contaminated with Listeria monocytogenes.
The company has not received test results for Listeria monocytogenes in connection with the recalled products, but due to recurring Listeria species issues at the firm, it has decided to remove the products from commerce as a precautionary measure. There have been no confirmed reports of illnesses or adverse reactions due to consumption of these products.
Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.
Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.
FSIS and Bar S are concerned that some product may be frozen and in consumers’ freezers.
Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
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