Tropique Assorted Fruit Jelly Bag 30/9pcs/ recall
Recalled by Comercial Mexicana · Bethpage, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may present a choking hazard.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
TROPIQUE ASSORTED FRUIT JELLY BAG 30/9PCS/10.06oz and TROPIQUE JELLY ANIMAL JAR 6/26OZ
Quantity: 1500 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.
1. TROPIQUE ASSORTED FRUIT JELLY 30/9PCS/10.6oz UPC: 732068496333 Best Before:09/17/2021 2. TROPIQUE JELLY ANIMAL TIGER JAR 6/26OZ UPC: 732068496050 Best by 1/18/2022 3. TROPIQUE JELLY ANIMAL OWL JAR 6/26OZ UPC: 732068496012 Best By 1/18/2022 4. TROPIQUE JELLY ANIMAL DUCK JAR 6/26OZ UPC: 732068495992 Best By 1/18/2022 5. TROPIQUE JELLY ANIMAL BEAR JAR 6/26OZ UPC: 732068496098 Best by: 1/18/2022 6. TROPIQUE JELLY ANIMAL PANDA JAR 6/26OZ UPC: 732068496036 Best By: 1/18/2022 7.TROPIQUE JELLY ANIMAL PIG JAR 6/26OZ UPC: 732068496074 Best By: 1/18/2022 8. TROPIQUE JELLY ANIMAL CAT JAR 6/26OZ UPC: 732068496111 Best by:1/18/2022
Where it was sold
Connecticut Florida New Jersey New York Pennsylvania
FDA's distribution note: NY, NJ, CT, PA, FL retail stores.
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
- Comercial Mexicana
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 22, 2020
- In FDA report of
- Nov 18, 2020
- Terminated
- Apr 6, 2022
- FDA recall number
- F-0110-2021 · event 86637
- Official record
- FDA enforcement report search