July 15, 2019

Sunstone Organics Kratom Recalled For Possible Salmonella

Sunstone Organics is recalling two lots of Sunstone Organics Kratom, including White Vein Kratom Lot 119 and Maeng Da Kratom Lot 124A. The recall covers both capsules and powder form, in all sizes. These products may be contaminated with Salmonella bacteria. No reports of illness have been received to date in connection with this recall. The product is used as a tea or a supplement and is packaged in Kraft stand-up pouches, in three different size bags. The package sizes in the powder type are 25 grams, 50 grams, and 100 grams. The package sizes in the capsule form are 20 count, 60 count, and 150 count. You can see the UPC numbers for these recalled products at the FDA web site. All six kratom sizes pertain to the same lot number. These kratom products do not have an expiration … [Read more...]

Kingston Pharma Recalls All Lots of DG Baby Gripe Water

Kingston Pharma, LLC is recalling all lots of "DG Baby Gripe Water" herbal supplement with organic ginger and fennel extracts because of an undissolved ingredient, citrus flavonoid. While this does not make the product hazardous in and of itself, but some people who are sensitive could have difficulty swallowing the water. The company has received one report of a one-week old infant having difficulty when swallowing the product. In addition, three complaints have been registered with the company because of the undissolved citrus flavonoid. The product claims to release discomfort from gas, colic, hiccups, and teething. This DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts is administered orally to infants and adults. The recalled product is packaged in 4 … [Read more...]

World Waters Recalls WTRMLN WTR For Foreign Material

World Waters is recalling some of their WTRMLN WTR beverages because it may contain foreign materials, more specifically pieces of soft plastic. The plastic is floating in some of the finished product. The company is using consumers to check the package before they open it and drink it. No adverse events have been reported to date in connection with this issue, but the plastic could be a choking hazard. The recalled product is WTRMLN WTR Original 12 packs in Watermelon Flavor. The lot number, printed on the bottom of the bottle, can be seen at the FDA web site.  The product label is printed to look like a watermelon, with a pink center surrounded by green and white stripe. These products were sent to customers nationwide for distribution in retail stores from December 22, 2018 … [Read more...]

Mountain Man Apple Cider Recalled for Possible E. coli Contamination

Mountain Man Market of Cana, Virginia is recalling 1/2 gallon containers of Mountain Man Apple Cider because it may be contaminated with E. coli bacteria, according to news reports. The bacteria is identified as Shiga toxin-producing E. coli (STEC), which can cause serious illness and hemolytic uremic syndrome (HUS), a kind of kidney failure. This recall is not listed on the FDA site. The recalled Mountain Man Apple Cider was distributed locally in Canada, Virginia at the Mountain Man Market on and before November 10, 2018. The product is packaged in a clear 1/2 gallon container. This cider has not been pasteurized, a process that destroys pathogenic bacteria. If you bought this product, do not drink it and do not use it to cook or bake. Discard it or return it to the store where you … [Read more...]

Regen Series Liveyon Product Recalled For Adverse Reactions

Regen Series Product, which is manufactured by Genetech, Inc., and distributed by Liveyon, LLC, is being recalled because adverse reactions have been reported to the FDA. Liveyon was notified by the Center for Biologics Evaluation and Research on Thursday, September 28, 2018 about this issue and was told about possible reported adverse reactions and concerns about products made by Genetech. These products are made from human cells and tissues. The recall notice did not state how these products are used, or what their intended use is. Liveyon has discontinued the purchase of any product from Genetch, suspended shipment of all product, and has found an alternative manufacturer. Meanwhile, all ReGen Series products are being recalled. Liveyon has also voluntarily recalled any Genetech … [Read more...]

Silver Star Homeopathic Meds Recalled for Possible Microbial Contamination

Silver Star Brands products are being recalled for possible microbial contamination. "The products have been tested and found to contain microbial contamination," according to the FDA recall notice. Use of these products could result in increased infections that could be life-threatening to some people. No adverse reactions have been reported in this recall. The recall is for six Silver Star Brands human products and two pet products. These products were distributed nationwide to retailers and to consumers through direct sales and the company's website. Six of the products are intended for human use, and two are intended for pet use. The recalled products are Native Remedies VertiFree oral spray with UPC number 818837012260, Native Remedies VaricoGo oral spray with UPC number … [Read more...]

Some Abbott Liquid Diet Products Recalled in Canada for Possible Bacterial Contamination

One illness has been reported associated with some Abbott Two Cal brand and Abbott Promote brand formulated liquid diet products in Canada. Those products are now subject to a recall. The products were sold nationwide at the retail level. This recall was triggered by consumer complaints. One illness has been reported to public health officials. The recall notice did not state what strain of bacteria may be in those products, and also did not state if any testing of the products has revealed the possible pathogen. The recalled products include Abbott Promote High-Protein Liquid Nutrition - Vanilla Flavor in 235 ml bottles. The code on the product is L84417RA0 xxxx (xxxx=time code) 2019JA1 and the UPC number is 0 55325 20170 0. Also recalled is Abbott Two Cal HN Complete, Balanced … [Read more...]

HelloLife Recalls Products For Microbial Contamination

HelloLife of Michigan is recalling four different products - Neuroveen, Respitrol, Thyroveev and Compulsin - for possible microbial contamination. Neuroveen has been tested and is contaminated with Staphylococcus saprophyticus and Burkholderia cepacia bacteria. Compulsin contains Burkholderia cepacia. The other two products are still pending bacterial identification. Administration or use of drug products with contamination could create infections that can be life-threatening. No reports of adverse events have been received by the company to date. All of these HelloLife products are packaged in 2 ounce amber bottles. The recalled products are Neuroveen, a natural temporary relief for nerve pain symptoms, with UPC number 891129002804, lot number NV/030717D, and expiration date 7/19; … [Read more...]

Pfizer Recalls Children’s Advil; Lily Bulb Recalled for Sulfites

Two product recalls were announced today: One for undeclared sulfites in "Lily Bulb", the other by Pfizer, recalling Children's Advil Suspensiuon Bubble Gum for incorrect dosage cup. The recall of Pfizer's Children's Advil Suspension Bubble Gum, Flavored was issued because of concerns of a possible ibuprofen overdose. The symptoms associated with this type of overdose includes nausea, vomiting, drowsiness, headache, dizziness, and blurred vision. The product was distributed nationwide to wholesales, distributors, and eretailers. The Children's Advil Suspension Bubble Gum Flavored product was sold in 4 ounce bottles, with NDC 0573-0207-30, and lot R51129. It was sold from May 2018 through June 2018. The SKU number is F005730207300, the UPC number is 3-0573-0207-30-0, and the … [Read more...]

King Bio Recalls Aqueous-Based Products for Microbial Contamination

King Bio is recalling all of its aqueous-based products for human and animal use for possible microbial contamination. The recall notice states, "Administration or use of drug products with microbial contamination, could potentially result in increased infections that may require medical intervention, and could result in infections that could be life threatening to certain individuals." No illnesses have been reported in connection with these products. These products are being recalled as "a precautionary measure," according to a statement by King Bio. The recall notice at the FDA web site contains a link to the recalled products. They include Acne Clear, Allergies & Hay Fever, Allergy: Rocky Mountains, Gout Symptom Formula, Grief & Guilt Reliever, Head Colds Relief, Stress … [Read more...]

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