Weekly Recall Notification

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Recall information from the Minnesota Department of Agriculture

October 24, 2023


Nature's Path Organic Foods Issues Allergy Alert

October 19, 2023 - Nature's Path Organic Foods of Vancouver, BC,  is voluntarily recalling specific batches of its Organic Pumpkin Spice Waffles and Organic Dark Chocolate Chip Waffles because they may contain trace amounts of undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected products were only sold in the USA. This issue is isolated to two batches of Organic Pumpkin Spice Waffles and Organic Dark Chocolate Chip Waffles with the following lot codes:

  • Nature's Path Organic Pumpkin Spice Waffles
    o Best Before Date: 2023 OCT 24 o Lot Code:
    2C110242 o UPC: 0 5844959077 4
  • Nature's Path Organic Dark Chocolate Chip
    Waffles o Best Before Date: 2023 OCT 26 o
    Lot Code: 2C110262 o UPC: 0 5844916701 3

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Greenhead Lobster Products Issues Recall

October 20, 2023 - Greenhead Lobster Products, of Bucksport, ME, is voluntarily recalling all frozen and refrigerated cooked lobster meat products produced from May 9, 2023, through October 19, 2023, due to the potential for the product to be contaminated by Listeria monocytogenes.

The recalled product, Greenhead Lobster Fresh Cooked Lobster Meat was sold frozen or refrigerated in packages ranging from 1 to 2 lbs. or in cases up to 12 lbs. and can be identified with “best if used by” dates ranging from May 9th, 2025, to October 12th, 2025, for frozen product, and May 27th, 2023, to October 30th, 2023, for refrigerated product. The “best if used by” date is located on the white label on the front of the package. Products under recall are listed in the accompanying table.

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Botanical-Be Issues Recall

October 22, 2023 - Botanical-Be of El Paso, TX,  is voluntarily recalling of all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has found the Kuka Flex Forte, capsules, Artri King, capsules, and Reumo Flex, capsules, to be tainted with Diclofenac. Diclofenac is an approved non-steroidal anti-inflammatory drug (NSAID), the presence of Diclofenac in Kuka Flex Forte, Artri King, and Reumo Flex renders them unapproved drugs for which safety and efficacy have not been established and, therefore, subject to recall. 

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department of agriculture


Please contact MDA Recall Coordinator Erin Smilanich at erin.smilanich@state.mn.us