Pride of Africa brand Farina
Reason Label review revealed the product contains undeclared wheat.
Pride of Africa brand Semo "Semolina" recall
Recalled by Raymond-Hadley Corp. · Spencer, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Label review revealed the product contains undeclared wheat.
Undeclared allergen: Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Pride of Africa brand Semo "Semolina", Net Wt. 5 lb., UPC 016712016918 --- A Product of Raymond-Hadley Corp. Spencer, NY 14883 1-800-252-5220
Quantity: 5,706 units
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/Codes: 7614, 10-26-12, 2/18/14 049147/30/13 = 1, 12514, 10-26-12 = 6, 3-18-13, 10/4/13 = 2, 125141, 12-26-12 = 9, 3-18-13 = 2, 9-13-12, 202141, 11/20/13, 4-24-13 = 4, 9-13-2012, 287141, 11413-1, 4-18-12, 7-30-13, 04914 2/18/14, 12-26-12, 4-24-13, 1/07/2014 -1, 07614 = 29, 139141 = 51, 4-24-13-1, 2/18/14 =1, 2/18/14-1= 8, 6-20-12 = 8, 1/7/14, 12514-1 = 1, 9-13-12 = 6, 10/4/13, 2/18/14, 7/30/13
Where it was sold
Delaware Georgia Illinois Massachusetts Maryland Maine New Jersey New York Texas
FDA's distribution note: DE, GA, IL, MA, MD, ME, NJ, NY, TX
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. 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
- Raymond-Hadley Corp.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 3, 2014
- In FDA report of
- Nov 19, 2014
- Terminated
- May 3, 2017
- FDA recall number
- F-0470-2015 · event 69646
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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