Recall record at a glance
| Official record | F-2438-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Swanson Health Products, Inc. |
| Report date | Sep 24, 2014 |
| Recall initiation date | Jul 28, 2014 |
| Quantity | 544 containers |
| Location | Fargo, ND, United States |
Official product description
Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High Density Poly-ethylene plastic containers, Product of Italy, Distributed by Swanson Health Products, PO Box 2803, Fargo ND 58108 USA, SWF115.
Why the product was recalled
Swanson Certified Organic Carob Powder, item number SWF115 is being recalled due to a potential risk of Salmonella contamination from a raw ingredient used in this product.
Distribution information
US: AL AK, AZ, AR, C,A CO, CT, DC, FL, HI ID, IL IN, IA, KS, KYT,LA, MD, MA, MI, MN, NS, NO, NT,NV, NJ, NM, NY, NC, ND, OH,OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WV, WI, WY. OUS: AUSTRALIA, SWEDEN, CANADA, MEXICO, KOREA, CHILE.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.