Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported July 25, 2012
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 lacta
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Standard Process, Inc. recalled SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 & 36… - a critical-severity action.
SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 & 36… was recalled by Standard Process, Inc. in July 25, 2012. Reason: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contaminati…. Check the official notice for the remedy. Verify recall #F-1765-2012 with the FDA Food before acting.
The recall
Standard Process, Inc. issued this critical-severity FDA Food recall-Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contaminati….
- Critical
- severity level
- Class I
- classification
- July 25, 2012
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1765-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1765-2012) was formally reported on July 25, 2012, with the manufacturer initiating the action on June 27, 2012. It is classified under Critical severity (Class I), with a current status of Terminated. Standard Process, Inc. is listed as the recalling firm, operating out of Palmyra, WI. Federal records list the affected scope as 23,874 bottles.
The documented reason for this recall is: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination. Distribution data in the federal record shows the product reached: 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.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
23,874 bottles
Related Recalls
6
6 from same agency
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.
Reason for recall
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1765-2012 |
| Date reported | July 25, 2012 |
| Date initiated | June 27, 2012 |
| Recalling firm | Standard Process, Inc. |
| Firm location | Palmyra, WI |
| Affected scope | 23,874 bottles |
| Distribution | 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. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1765-2012) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Standard Process, Inc.. Units affected: 23,874 bottles.
Why was this product recalled? ▼
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 25, 2012. Severity: Critical. Recall number: F-1765-2012.
Where was the recalled product distributed? ▼
Distribution: 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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1765-2012) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 25, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.