Food Recall Check
Class I · High risk Terminated Initiated Jun 27, 2012 (14 years ago)

Standard Process Pancreatrophin PMG recall

Recalled by Standard Process, Inc. · Palmyra, WI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Standard Process, Pancreatrophin PMG (Product # 6650), 90 Tablets, Proprietary Blend: Bovine pancreas PMG extract, dried alfalfa (whole plant) juice, nutritional yeast, porcine duodenum, deflated wheat (gem) , dried buckwheat (leaf) juice and buckwheat (seed). Other Ingredients: Arabic gum and calcium stearate. Standard Process Inc., PO Box 904, Palmyra, WI 59158, UPC 8 12122 01153 2 12.

Quantity: 12,422 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 114, Best Used By dates of 05/13.

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut District of Columbia Delaware Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina Nebraska New Hampshire New Mexico Nevada New York Ohio Oklahoma Pennsylvania Rhode Island South Carolina Tennessee Texas Virginia Vermont Washington Wisconsin West Virginia

FDA's distribution note: AL, AZ, AR, CA,CO, CT, DE, DC, FL,GA, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NV, NY, NH,NM, NY, NC, OH, OK, PA, RI,SC, TN,TX,VT, VA, WA, WV, WI.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Standard Process, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 27, 2012
In FDA report of
Jul 25, 2012
Terminated
Jan 13, 2014
FDA recall number
F-1766-2012 · event 62477
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class I · High risk Terminated Salmonella

SP Standard Process

Reason Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

Standard Process, Inc. 41 states F-1764-2012
Class I · High risk Terminated Salmonella

SP Standard Process

Reason Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

Standard Process, Inc. 41 states F-1765-2012

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