Recall information from the Minnesota Department of Agriculture
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January 18, 2018 – Bulletproof 360, Inc. is recalling Bulletproof Collagen Protein dietary supplement due to undeclared milk.
The recalled product is Bulletproof Collagen Protein dietary supplement, packaged in a 16-oz. composite-film bag and has the UPC 8 15709 02115 3. The affected lot #1017088 EXP03/19 is found on the back panel of a bag, and EXP03/19 means expires by March 2019.
Affected Bulletproof Collagen Protein was distributed to retail stores nationwide.
Consumers who have purchased the affected product (lot # 1017088) and have an allergy or severe sensitivity to milk are urged not to consume it and should return product to the original location of the purchase for a full refund.
Consumers with questions related to the recall can contact our Customer Support Team at: support@bulletproof.com or reach out to us via phone at: (877) 651-9482, Monday through Friday, 8:00 am - 5:00 pm Pacific Standard Time.
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January 22, 2018 – Sun Noodle is voluntarily recalling one lot of their retail Tonkotsu Ramen because it is mis-labeled. While it is labeled Tonkotsu, the actual flavor packet inside is Assari Shoyu, which contains an additional undeclared allergen of fish (sardines).
The product is packaged in a clear plastic clamshell, banded with a Sun Noodle label that reads "Tonkotsu Ramen." The affected product contains 2 purple and white soup base packets, which correctly show the name "Assari Shoyu" flavor. The products affected by the recall are labeled with lot code 3217332.
Consumers who have purchased any of the affected lot of Tonkotsu Ramen are urged to return the product to the original location of the purchase for a full refund. Consumers with questions may contact a toll free number at the company: 1-866-366-6353, Monday through Friday, 8:30 am - 5:30 pm Hawaii Standard Time.
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January 21, 2018 – Break Ventures/California Basics is recalling its Dietary Supplement “Zero for Him 150ct” because it may be contaminated with Salmonella.
The Product was distributed nationwide through Amazon. It comes in a 400cc, Light Amber PETE bottle marked with lot #1710-638 on the bottom and with an expiration date of November 2020 stamped on the side.
Distribution of the Product has been suspended while FDA and the company continue their investigation as to the source of the Salmonella.
Consumers who have purchased Zero for Him Lot#1710-638 are urged to return them to the place of purchase for a full refund. Consumers with additional questions may contact the company at 323-375-5953.
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January 21, 2018 – Arthri-D, LLC is recalling its Dietary Supplement “Arthri-D 120ct” because it may be contaminated with Salmonella.
The Product was distributed nationwide through mail orders. It comes in a 225 cc, white plastic HDPE bottle marked with lot #1701-092 on the label and with a manufacturing date of March 2017 stamped on the side.
Distribution of the Product has been suspended while FDA and the company continue their investigation as to the source of the Salmonella.
Consumers who have purchased 120 count of Arthri-D lot#1701-092 are urged to return them to the place of purchase for a full refund. Consumers with additional questions may contact the company at 978-992-0505
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January 19, 2018 – Ottogi America, Inc. is recalling “Rice cake soup” food, because it may contain undeclared milk.
The recalled “Rice Cake Soup” was distributed nationwide in retail stores. The product comes in a 6.40 ounce, yellow paper bowl package marked with Item No: 29409101 on the back with an expiration date of June 20th 2018 stamped under the case.
Production of the product has been suspended until FDA and the company are certain that the problem has been corrected.
Consumers who have purchased 6.40 ounce packages of "Rice cake soup" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-310-324-1094. (Monday – Friaday from 8:00AM to 5:00PM PST)
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January 19, 2018 – In accordance with a Consent Decree of Permanent Injunction ordered in the United States District Court for the District of New Jersey, Flawless Beauty, LLC is recalling all lots of nineteen different products sold individually or as part of multi-unit kits alleged by the U.S. Food and Drug Administration ("FDA") to be misbranded or unapproved new drugs pursuant to the Federal Food, Drug, and Cosmetic Act. The FDA believes that these drugs present serious public health risks.
The products subject to the recall were sold and distributed over the Internet to U.S. and foreign customers. The web site of Flawless Beauty is www.flawlessbeautyandskin.com. All glutathione products were sold in multi-vial whitening kits, either alone or in combination with ampules of vitamin C and sterile water. Vials or ampules of vitamin C or sterile water purchased separately or as part of these whitening kits are also recalled. for full list of recalled products click here.
Consumers with questions regarding this recall can contact Flawless Beauty by phone at 1-917-831-5948 or jack@flawlessbeautyandskin.com on Monday-Friday, 9:30AM – 5:30 PM, EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these products.
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Questions?
Please contact MDA Recall Coordinator Alida Sorenson at alida.sorenson@state.mn.us
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