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Class III: unlikely to cause harmTerminated

Swanson Recall

Swanson, Premium Brand, Full Spectrum Black Cumin Seed (Nigella Sativa) Dietary Supple…

Swanson Health Products, Inc · Fargo, ND

Risk level
Class III
Reported by FDA
Nov 27, 2013
Recall ID
F-0220-2014
Check your lot numberHow we source this data

Summary

Swanson Health Products recalled Swanson starting Sep 26, 2013. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0220-2014 on Nov 27, 2013. Reason: Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativa) Dietary Supplement Capsules. The product was found to be mislabel. Bottles of Black Cumin Seed from these two lots numbers (199399 & 201359) have been found to contain White Cumin Seed (Cuminum cyminum). Status: Terminated.

Why it was recalled

Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativa) Dietary Supplement Capsules. The product was found to be mislabel. Bottles of Black Cumin Seed from these two lots numbers (199399 & 201359) have been found to contain White Cumin Seed (Cuminum cyminum).

Product description

Swanson, Premium Brand, Full Spectrum Black Cumin Seed (Nigella Sativa) Dietary Supplement capsules, 400 mg, SW1361, UPS 0 87614 11361 6.

Lot numbers, UPCs & expiration codes

199388, 201359

Where it was sold

US: nationwide. OUS: Australia,,Taiwan, England, Portugal, Denmark, Hong Kong, Bahrain, Thailand, Ireland, France, Poland, Macedonia, Brunei, United Arab Emirates, Israel, Japan.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0220-2014
Classification
Class III
Status
Terminated
Recall initiated
Sep 26, 2013
FDA report date
Nov 27, 2013
Quantity
3689
Recall type
Voluntary: Firm initiated
Recalling firm
Swanson Health Products, Inc

Original FDA data

Every field from FDA enforcement report F-0220-2014, exactly as published.

Show all FDA fields
City
Fargo
State
ND
Status
Terminated
Country
United States
Event ID
66665
Address
4075 40th Ave S
Code information
199388, 201359
Postal code
58104-3912
Report date
Nov 27, 2013
Product type
Food
Recall number
F-0220-2014
Classification
Class III
Recalling firm
Swanson Health Products, Inc
Product quantity
3689
Termination date
Jun 2, 2014
Reason for recall
Swanson Health Products is recalling two lots of Swanson Premium Full Spectrum Black Cumin Seed (Nigella sativa) Dietary Supplement Capsules. The product was found to be mislabel. Bottles of Black Cumin Seed from these two lots numbers (199399 & 201359) have been found to contain White Cumin Seed (Cuminum cyminum).
Voluntary / mandated
Voluntary: Firm initiated
Product description
Swanson, Premium Brand, Full Spectrum Black Cumin Seed (Nigella Sativa) Dietary Supplement capsules, 400 mg, SW1361, UPS 0 87614 11361 6.
Distribution pattern
US: nationwide. OUS: Australia,,Taiwan, England, Portugal, Denmark, Hong Kong, Bahrain, Thailand, Ireland, France, Poland, Macedonia, Brunei, United Arab Emirates, Israel, Japan.
Recall initiation date
Sep 26, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 20, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0220-2014, published Nov 27, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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