SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360…
Recalling firm: Standard Process, Inc.
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 13, 2014.
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FDA code information
Lot 114, Lot 114, Best Used By dates of 05/13.
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Full FDA record and distribution details
Original 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.
Original FDA recall reason
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Recall details
- Recall number
- F-1764-2012
- Event ID
- 62477
- FDA status
- Terminated
- Initiated
- Jun 27, 2012
- Reported
- Jul 25, 2012
- Classified
- Jul 16, 2012
- Terminated
- Jan 13, 2014
- Quantity
- 29,044
- Location
- Palmyra, WI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
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.
Data updated September 16, 2026. View official FDA data ↗
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