Drug recall
SP Standard Process, Cataplex ACP (Product #0700 and 0750), Dietary supplement, 90 & 360 Tablets, Proprietary…
FDA recall event 62477 · Class I · Standard Process, Inc.
Key facts
| Event ID | 62477 |
|---|---|
| Recall numbers | F-1764-2012, F-1765-2012, F-1766-2012 |
| Recalling firm | Standard Process, Inc. |
| Product type | Food |
| Products | 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…, 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…, Standard Process, Pancreatrophin PMG (Product # 6650), 90 Tablets, Proprietary Blend: Bovine pancreas PMG extract, dried alfalfa (whole plant) juice, nutritional yeast, porcine duodenum, deflated… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination. |
| Initiation date | Jun 27, 2012 |
| Report date | Jul 25, 2012 |
| Termination date | Jan 13, 2014 |
| City | Palmyra |
| State | WI |
| Country | United States |
| FEI number | 2120780 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: