Steamable by Lidl Chopped Spinach
Reason Possible contamination of Listeria monocytogenes in frozen chopped spinach.
Giant Eagle Diced Green Peppers recall
Recalled by Frozen Food Development · Rheems, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Frozen Food Development, Lancaster, PA is initiating a recall of Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases (12/10 oz. bags per case) and bulk 22 lbs. bags because they tested positive for 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
Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases, also poly bags and cartons, 12/10 oz. bags per case and bulk 22 lbs. bags
Quantity: 20,825 lbs.
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.
R16372 exp. 03/12/2023 R16514 exp. 09/30/2022 R17422 exp. 01/21/2023 R17117 exp.. 08/12/2023 R17133 exp. 04/14/2023 R18388 exp. 10/14/2023
Where it was sold
FDA's distribution note: The product was distributed to three direct Accounts in the United States.
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. 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
- Frozen Food Development
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 30, 2021
- In FDA report of
- Jan 5, 2022
- Terminated
- Sep 22, 2022
- FDA recall number
- F-0356-2022 · event 89148
- Official record
- FDA enforcement report search