NeolifeBar Fruit & Nuts recall
Recalled by Natural Formulas · Hayward, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product was manufactured with Sunflower Kernels provided by SunOpta, which are under recall for possible contamination with Listeria Monocytogenes.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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
NeolifeBar: Fruit & Nuts; 10 g Protein; 5 g Fiber. 320 mg Omega-3s. Net Wt. 1.6 oz. (45 g). Product is sold as a package of 15 bars: Distributed by GNLD International, LLC, Fremont, CA. Not sold in retail stores
Quantity: 309 cases in US, 4384 cases foreign distribution
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 3285A, (US and foreign distribution) Best By 12/2016 and lot 3425A and 0476A (foreign distribution only.
Where it was sold
FDA's distribution note: US and Mexico, Finland, Estonia, Japan, Italy, Finland, Japan, South Africa.
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
- Natural Formulas
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 23, 2016
- In FDA report of
- Oct 5, 2016
- Terminated
- Oct 19, 2016
- FDA recall number
- F-2154-2016 · event 74543
- Official record
- FDA enforcement report search