Sebastiano s Naturally Flavored Gourmet Syrups French Vanilla Naturally Sugar Free
Reason The front panel of the affected products states Naturally Sugar Free, but the product contains sugar.
Sebastiano's Naturally Flavored Gourmet Syrups Hazelnut recall
Recalled by Frutarom USA Inc. · West Chester, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Hazelnuts are not declared in the ingredient statement or in a contains statement.
Undeclared allergen: Tree nuts
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
Sebastiano's Naturally Flavored Gourmet Syrups Hazelnut 25.4 fl oz (750 ml)
Quantity: 17,274 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.
5047192, 5073855, 5086313, 5097374, 5105739, 6132322, 6147917, 6154983, 6166859, 6173856, 6181440, 6191867, 6204636, 6217598, 6225567, 6237631, 6247601, 7262755, 7270152, 7289634, 7313494, 7327963, 8404772, 8436885, 8447506, 8457444, 8458028
Where it was sold
Massachusetts
FDA's distribution note: Distributed to one firm in MA.
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 tree nuts; 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
- Frutarom USA Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 28, 2018
- In FDA report of
- Dec 19, 2018
- Terminated
- Jul 26, 2019
- FDA recall number
- F-0714-2019 · event 81692
- Official record
- FDA enforcement report search