National Heartland Naturals Premium Quality Pearl Barley
Reason Product was labeled as gluten free by mistake, but the product does contain Gluten.
Bedessee Brown Betty BRAND COCONUT MILK Powder Mix recall
Recalled by Bedessee Imports, Inc · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Canadian Food Inspection Agency processed a recall involving Brown Betty brand Coconut Milk Powder Mix which contains sodium caseinate but lacks "milk" declaration.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Bedessee Brown Betty BRAND COCONUT MILK Powder Mix, NET WT: 1) 1.76 OZ (50 g) and 2) 10.6 OZ. IMPORTED BY BEDESSEE IMPORTS LTD. Brooklyn, NY USA 11208. PRODUCT OF VIETNAM.
Quantity: 344 cartons (316 cartons/1.76 oz & 28 cartons/10.6 oz) (76 cartons are quarantined)
Food: Milk & dairy
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.
none
Where it was sold
Connecticut Florida Maryland North Carolina New Jersey New York
FDA's distribution note: NY, NJ, CT, MD, NC via retail stores and one FL site
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
- Bedessee Imports, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 26, 2015
- In FDA report of
- Jul 15, 2015
- Terminated
- Jun 13, 2018
- FDA recall number
- F-2841-2015 · event 71326
- Official record
- FDA enforcement report search
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