Exact FDA event identifier

Event 62477

3 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: June 27, 2012
Product types: Food
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Standard Process, Inc.

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 3

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.

F-1764-2012

Recall number: F-1764-2012
Initiated: June 27, 2012
Classification: Class I
Status: Terminated
Recalling firm: Standard Process, Inc.
Quantity: 29,044

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

Salmonella contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

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.

food · product 2 of 3

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.

F-1765-2012

Recall number: F-1765-2012
Initiated: June 27, 2012
Classification: Class I
Status: Terminated
Recalling firm: Standard Process, Inc.
Quantity: 23,874 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

Salmonella contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

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.

food · product 3 of 3

Standard Process, Pancreatrophin PMG (Product # 6650), 90 Tablets, Proprietary Blend: Bovine pancreas PMG extract, dried alfalfa (whole plant) juice, nutritional yeast, porcine duodenum, deflated wheat (gem) , dried buckwheat (leaf) juice and buckwheat (seed). Other Ingredients: Arabic gum and calcium stearate. Standard Process Inc., PO Box 904, Palmyra, WI 59158, UPC 8 12122 01153 2 12.

F-1766-2012

Recall number: F-1766-2012
Initiated: June 27, 2012
Classification: Class I
Status: Terminated
Recalling firm: Standard Process, Inc.
Quantity: 12,422 bottles

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

Salmonella contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

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.