SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 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 C, Dietary Supplement, (Product # 1650 and 1655) , 90 & 360 Tablets, Proprietary Blend: Veal bone PMG extract, bovine adrenal, dried buckwheat (leaf) juice, buckwheat (seed), nutritional yeast, dried alfalfa( whole plant) juice, alfalfa flour, mushroom , magnesium citrate, bovine bone, deflated wheat (germ), calcium acid phosphate, Echinacea(root), carrot (root), veal bone, soybean lecithin, mixed tocopherols (soy , and rice (bran)., Other Ingredients calcium lactate, honey, aerola (berry), camu camu (berry), manloc (root), calcium stearate, and arabic gum, UPC 8 12122 01029 0 16.
Original FDA recall reason
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Recall details
- Recall number
- F-1765-2012
- Event ID
- 62477
- FDA status
- Terminated
- Initiated
- Jun 27, 2012
- Reported
- Jul 25, 2012
- Classified
- Jul 16, 2012
- Terminated
- Jan 13, 2014
- Quantity
- 23,874 bottles
- 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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