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Class I: serious health riskTerminated

Standard Process SP Standard Process Recall

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 &…

Standard Process, Inc. · Palmyra, WI

Risk level
Class I
Reported by FDA
Jul 25, 2012
Recall ID
F-1764-2012
Check your lot numberHow we source this data

Summary

Standard Process recalled SP Standard Process starting Jun 27, 2012. The FDA classified it as Class I (serious health risk) and published enforcement report F-1764-2012 on Jul 25, 2012. Reason: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

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

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1764-2012
Classification
Class I
Status
Terminated
Recall initiated
Jun 27, 2012
FDA report date
Jul 25, 2012
Quantity
29,044
Recall type
Voluntary: Firm initiated
Recalling firm
Standard Process, Inc.

Original FDA data

Every field from FDA enforcement report F-1764-2012, exactly as published.

Show all FDA fields
City
Palmyra
State
WI
Status
Terminated
Country
United States
Event ID
62477
Address
1200 W Royal Lee Dr
Code information
Lot 114, Lot 114, Best Used By dates of 05/13.
Postal code
53156-9209
Report date
Jul 25, 2012
Product type
Food
Recall number
F-1764-2012
Classification
Class I
Recalling firm
Standard Process, Inc.
Product quantity
29,044
Termination date
Jan 13, 2014
Reason for recall
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
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.
Recall initiation date
Jun 27, 2012
Initial firm notification
Letter
Center classification date
Jul 16, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1764-2012, published Jul 25, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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