CLASS I Food recall · Reported 25 Jul 2012 · FDA Enforcement Report
SP Standard Process, Cataplex C, Dietary Supplement recalled
Standard Process is recalling SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 &, distributed in 41 states. The recall was initiated on 27 Jun 2012 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1765-2012
- FDA event ID
- 62477
- Recalling firm
- Standard Process, Palmyra, WI
- Brand
- SP Standard
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 27 Jun 2012
- FDA classified
- 16 Jul 2012
- Reported
- 25 Jul 2012
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Salmonella
- Product category
- Herbal Supplements
Timeline
| 27 Jun 2012 | Recall initiated by company | |
| 16 Jul 2012 | Classified by FDA | +19 days |
| 25 Jul 2012 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
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.
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.
AlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaIowaIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMichigan
Questions about this recall
Is SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 & recalled?
Yes. Standard Process recalled SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 & on 27 Jun 2012. The recall is Class I and its status is Terminated. Recall number F-1765-2012.
Why was it recalled?
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
Which lots are affected?
Lot 114, Lot 114, Best Used By dates of 05/13.
Where was it 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 should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Standard Process
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Standard Process, Pancreatrophin PMG (Product # 6650) recalledStandard Process | Standard Process | Salmonella | 41 states |
| Food | CLASS I | SP Standard Process, Cataplex ACP (Product #0700 and 0750) recalledSP Standard | Standard Process | Salmonella | 41 states |
Other Herbal Supplements recalls
All 509| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Lacnola; Small recalled by The Hampton Grocer | The Hampton Grocer | Salmonella | Nationwide |
| Food | ANNOUNCED | Moringa Leaf Powder recalled by Foods AliveFoods Alive | Foods Alive | Salmonella | Nationwide |
| Food | CLASS II | A-L Complex Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-P Herbal Supplement May Contain Nuts recalled by Byron White FormulasByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |
| Food | CLASS II | A-fng Herbal Supplement May Contain Nuts recalledByron | Byron White Formulas | Undeclared Tree Nuts | 50 states |