Swanson Ultra
Reason Dietary supplement may contain potential metal shavings greater than or equal to 7mm in length.
Swanson Full Spectrum Cilantro recall
Recalled by Swanson Health Products, Inc · Fargo, ND, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The contract manufacturer has notified Swanson Health Products that Swanson Full Spectrum Cilantro (Coriander) (SW1112) is subject to a recall due to a potential risk of salmonella contamination.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Swanson Full Spectrum Cilantro (Coriander) Herbal Supplement, 60 capsules, 425 mg, SW1112. UPC 87614-11112
Quantity: 3,419 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 203921 and 204888 each with MFG Date 11/2013
Where it was sold
Nationwide.
FDA's distribution note: nationwide
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Swanson Health Products, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 28, 2014
- In FDA report of
- May 21, 2014
- Terminated
- Sep 15, 2014
- FDA recall number
- F-1936-2014 · event 67968
- Official record
- FDA enforcement report search
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