--- title: Vegetables Recalled over Listeria Risk date: 2019-11-08T15:46:34-08:00 author: Bill Marler canonical_url: "https://marlerclark.com/news_events/vegetables-recalled-over-listeria-risk" section: News --- [All News](/news_events) / [Outbreaks](https://marlerclark.com/news_events/outbreaks) / # Vegetables Recalled over Listeria Risk Mann Packing Co., Inc. announced today the voluntary recall of a series of vegetable products sold to select retailers in the United States and Canada. The voluntary recall is a response to a notification by the Food and Drug Administration and the Canadian Food Inspection Agency of a potential contamination with *Listeria monocytogenes*. To date, public health officials have not reported any illness associated with these products. Mann Packing is issuing this recall out of an abundance of caution. *Listeria monocytogenes* is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, *Listeria* infection can cause miscarriages and stillbirths among pregnant women. Mann Packing will continue to work closely with the authorities to investigate the issue. The recalled products have “Best If Enjoyed By” date of October 11, 2019 to November 16, 2019. The full list of products and all corresponding product images are available at [https://mannpackingproductlist11-2019.us](https://mannpackingproductlist11-2019.us/)[External Link Disclaimer](http://www.fda.gov/about-fda/website-policies/website-disclaimer) and [https://mannpackingproductlist11-2019.ca](https://mannpackingproductlist11-2019.ca/)[External Link Disclaimer](http://www.fda.gov/about-fda/website-policies/website-disclaimer) GHNW, LLC of Clackamas, OR is voluntarily recalling Mushroom Stir Fry Blend 10 oz. tray and Stir Fry Blend 16 oz. tray that were produced using Broccoli Slaw that is being recalled by Mann Packing Co., Inc. due to the potential to be contaminated with *Listeria monocytogenes*. *Listeria monocytogenes* is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, *Listeria* infection can cause miscarriages and stillbirths among pregnant women. At this time, we are not aware of any illnesses linked by health officials to this recall. No other GHNW, LLC products are affected by this recall. GHNW, LLC is issuing this recall out of an abundance of caution. The recalled products have “Sell By” dates of October 27, 2019 to November 8, 2019, which can be found printed in black ink on the front label of the product. The products affected were sold at QFC and/or Fred Meyer in Oregon and Washington State. The products are being recalled because they have the potential to be contaminated with *Listeria monocytogenes*. This recall is connected to a voluntary recall of vegetable products announced by Mann Packing Co., Inc. on November 3 after they were notified by the Food and Drug Administration and the Canadian Food Inspection Agency of potential contamination. How to identify the recalled product: 1. Veggie Power Blend Sold on the Self-Serve Cold Bar between 9/29/2019 and 11/04/2019 Tofu Shiitake Slaw Sold on the Self-Serve Cold Bar between 9/29/2019 and 11/04/2019 Viatrexx Bio Incorporated, Newark, Delaware is voluntarily recalling 10 mL sterile injectable vials of products, listed in the table below with lot numbers, to the consumer level. The products were sold exclusively to practitioners for office use. The products were manufactured in a manner that cannot guarantee its sterility. Administration of a non-sterile product, intended to be sterile, may result in a site-specific or systemic infection, which in turn may cause hospitalization, significant morbidity, or a fatal outcome. To date, Viatrexx has not received any reports of adverse events related to this recall. The products are used as sterile injectables and packaged in a 10 mL vial. The affected lots are included in the table. Lot #ExpProductNDC #19-S00001May: 2020Connectissue73069-100-4119-S00002May: 2020Muskel-Neural73069-347-4119-S00003May: 2020Ouch73069-402-4119-S00004May: 2020it hurts73069-270-4119-S00005May: 2020Adipose73069-024-4119-S00007May: 2020Systemic Detox73069-500-4119-S00008May: 2020Articula73069-037-4119-S00010May: 2020Neuro 373069-373-4119-S00012May: 2020Infla73069-249-4119-S00014May: 2020Collagen73069-095-4119-S00016May: 2020Prolo73069-443-4119-S00017May: 2020Lymph 173069-310-4119-S00018May: 2020Mesenchyme73069-102-4119-S00019May: 2020GI73069-189-4119-S00021May: 2020Arthros73069-035-4119-S00023May: 2020Immunexx73069-244-4119-S00024May: 2020Relief +73069-450-4119-S00025May: 2020Intra-Cell73069-250-4119-S00026May: 2020Facial73069-164-4119-S00020May 2020Neuro73069-375-4119-S00022May 2020Male +73069-320-4119-S00009May 2020Hair73069-206-4119-S00027May 2020ANS/CNS73069-039-41These products have a very limited distribution to less than 32 US practitioners. 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