FDA recall record

Standard Process Cataplex ACP recall — FDA F-1764-2012

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

Class Iclassification
F-1764-2012official record ID
Jul 25, 2012report date

Recall record at a glance

Official recordF-1764-2012
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmStandard Process, Inc.
Report dateJul 25, 2012
Recall initiation dateJun 27, 2012
Quantity29,044
LocationPalmyra, WI, United States

Official product description

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend: Dried buckwheat ( leaf) juice, buckwheat (seed), carrot (root), calcium lactate, nutritional yeast, bovine adrenal, bovine kidney, alfalfa flour, dried alfalfa, (whole plant) juice, magnesium citrate, mushroom, bovine bone, Echinacea (root, deflated wheat, (germ), oat flour, soybean lecithin, yeast bone, calcium acid, phosphate, mixed tocopherols, (soy), rice (bran), and carrot oil., Other ingredients: Honey ascorbic acid, calcium stearate, arabic, gum, starch, sucrose, vitamin A palmate., UPC 8 12122 01003 0 18.

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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