RecallRadar

FDA Food recall F-1764-2012

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend: Dried buckwheat ( lea…

On 2012-07-25 the FDA classified a Class I recall of SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend: Dried buckwheat ( lea… by Standard Process, citing standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

Read the official FDA Food notice

AgencyFDA Food
Recall numberF-1764-2012
ClassificationClass I
Statusterminated
Initiated2012-06-27
Published2012-07-25
Last updated2026-09-13 11:48 UTC
CompanyStandard Process
DistributionAL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NM, NV, NY, OH, OK, PA, RI, SC, TN, TX, VA, VT, WA, WI, WV

Product

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.

Reason

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

Identifiers

upc81212201003018
code_infoLot 114, Lot 114, Best Used By dates of 05/13.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1764-2012%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.