Wish Bone House Italian Salad Dressing
Reason The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.
Birds Eye Baby Sweet Peas recall
Recalled by Pinnacle Food Group, Llc · Cherry Hill, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product 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
Birds Eye Baby Sweet Peas, Net Wt. 13 oz. (369g ), Keep Frozen. UPC 14500-02253.
Quantity: 24,690 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.
Case Lot Numbers: 3905079AB1 and 3906079AB1, Retail Package Best By: JUL-06-19 and JUL-05-19
Where it was sold
Nationwide.
California Colorado Connecticut Florida Georgia Illinois Indiana Kentucky Massachusetts Maryland Maine Minnesota North Carolina North Dakota Nebraska Ohio Pennsylvania South Carolina Virginia Wisconsin West Virginia
FDA's distribution note: Nationwide - CT, CA, CO, FL, GA, IN, IL, KY, MA, MD, ME, MN, NC, ND, NE, OH, PA, SC, WV, VA, WI
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
- Pinnacle Food Group, Llc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 29, 2017
- In FDA report of
- Oct 18, 2017
- Terminated
- May 30, 2019
- FDA recall number
- F-0021-2018 · event 78206
- Official record
- FDA enforcement report search