IQF Cut Green Beans recall
Recalled by JML Ingredients · East Petersburg, PA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
JML Ingredients, Inc. of East Petersburg, PA is recalling IQF Cut Green Beans, because it has the potential to be contaminated 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
IQF Cut Green Beans; Net Weight 20 lb; Dist. by JML Ingredients, East Petersburg PA, 17520; Packed by: The International Co. for Agri Production & Processing. - ICAPP; Exporter's Address Industrial Zone A - 2 (Lot W) - 10th of Ramadan City - Egypt.
Quantity: 5473 - 20 lb. 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.
Lot number; Expiration date 110815/15649; August 10, 2017; 120815/15650; August 11, 2017; 050915/15651; September 4, 2017; 200915/15652; September 19, 2017
Where it was sold
Massachusetts Pennsylvania
FDA's distribution note: MA; PA
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
- JML Ingredients
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 22, 2016
- In FDA report of
- Mar 8, 2017
- Terminated
- Jun 2, 2017
- FDA recall number
- F-1537-2017 · event 74813
- Official record
- FDA enforcement report search