Candy Sweet Spots
Reason Bee International is recalling Sweet Spots Candy because it has undeclared egg allergen.
Plastic Heart Tubes with Chocolate Lentils recall
Recalled by Bee International, Inc. · Chula Vista, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Bee International is recalling Plastic Heart Tubes with Chocolate Lentils because they may contain undeclared milk protein.
Undeclared allergen: Milk
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
Plastic Heart Tubes with Chocolate Lentils, Net Wt. 1.7oz (48g), UPC 0-73563-00805-9, 24 count tubes per case
Quantity: 3427 cases
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.
Best Before April 2019
Where it was sold
Alabama California Florida Illinois Missouri North Carolina Ohio Tennessee Texas Virginia Vermont Washington Wisconsin
FDA's distribution note: US: AL, FL, TX, WI, VT, NC, VA, TN, WA, CA, OH, MO, IL
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. The risk from an undeclared allergen is to people allergic to milk; 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
- Bee International, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 20, 2017
- In FDA report of
- Mar 22, 2017
- Terminated
- May 31, 2017
- FDA recall number
- F-1595-2017 · event 76522
- Official record
- FDA enforcement report search