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RECALL RECORD — CLASS IRecall closedF-1764-2012/FDA enforcement
Standard Process, INC.·Dietary Supplements·Jun 27, 2012

Sp Standard Process, Cataplex Acp (Product #0700 and 0750), Dietary Supplement, 90 & 360…

What you need to know

Class I

  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDAAL, AZ, AR, CA +37 moreMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameStandard Process, INC.
Recalling firmStandard Process, INC.Palmyra, WI, United States
UPC / barcodes
81 212201 00301 8
Lot / date codes
  • Lot 114, Lot 114, Best Used By dates of 05/13.
Distribution area
ALAZARCACOCTDEDCFLGAILINIAKSKYLAMEMDMAMIMNMSMONENVNYNHNMNCOHOKPARISCTNTXVTVAWAWVWI

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.

United States

Quantity affected29, 044
Recall initiationFDA report date: July 25, 2012
FDA recall numberF-1764-2012

Beyond the headline

The recall, in context

Standard Process, INC. initiated this supplements recall on June 27, 2012. The FDA enforcement report states: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

Sp Standard Process, Cataplex Acp (Product #0700 and 0750), Dietary Supplement, 90 & 360… was made or distributed by Standard Process, INC. in Palmyra, WI, United States. This page reflects FDA report F-1764-2012, dated July 25, 2012.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Salmonella

Symptoms to watch for

Diarrhea, fever, abdominal cramps, nausea and sometimes vomiting. Symptoms can be severe in young children, older adults and immunocompromised people.

When symptoms may appear

Usually 6 hours to 6 days after exposure; illness often lasts 4 to 7 days.

Higher-risk groups

Children under 5, adults over 65, pregnant people and anyone with a weakened immune system are more likely to develop severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Sp Standard Process, Cataplex Acp (Product #0700 and 0750), Dietary Supplement, 90 & 360… recall?

Standard Process, INC. recalled Sp Standard Process, Cataplex Acp (Product #0700 and 0750), Dietary Supplement, 90 & 360… in an FDA Class I enforcement action reported as F-1764-2012. Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Standard Process, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1764-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Standard Process, INC.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.