Recall record at a glance
| Official record | F-2200-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | National Frozen Foods Corporation |
| Report date | Sep 21, 2016 |
| Recall initiation date | Jun 13, 2016 |
| Quantity | approximately 665,858 lbs. |
| Location | Moses Lake, WA, United States |
Official product description
Not Ready to Eat, IQF Peas and Carrots. Products' labels contains Cooking Instructions. Bountiful Harvest Peas & Carrots, item # 22486-11902, case & label UPC 30822486119028, Net wt. 12/2.5 LB Bountiful Harvest Peas & Carrots, item # 22486-11913, case & label UPC 00822486119133, Net wt. 30 LB C.H. Belt's Worlds Finest Peas & Carrots, item # WFN99-12490, case & label UPC 0088240000268, net wt. 20 LB Crown Point Peas & Carrots, item # CNP99-11241, case & label UPC 10813973016083, net wt. 20 LB James Farm Peas & Carrots, item # 60695-01001, case & label UPC 760695010011 and 6069501001, net wt. 12/2.5 LB Maplewood Peas & Carrots, item # 15429-23600, case & label UPC 81542923600, net wt. 12/2 LB Restaurant Saver Peas & Carrots, item # 60695-00353, case & label UPC 760695003532, net wt. 20 LB Smart Source Peas & Carrots, item # 22486-11916, case & label UPC 30822486116165, net wt. 12/2.5 LB Sysco Classic Peas & Carrots, item # 74865-07850, case & label UPC 10074865078501 and 7486507850, net wt. 12/2.5 LB Sysco Classic Peas & Carrots, item # 74865-66491, case & label UPC 00074865664912, net wt. 30 LB Sysco Reliance Peas & Carrots, item # 74865-65716, case & label UPC 00074865657167, net wt. 30 LB Valamont Peas & Carrots, item # 72608-12490, case & label UPC 00072608124907, net wt. 20 LB
Why the product was recalled
Not Ready To Eat IQF Peas and Carrots are recalled because they have a potential to be contaminated with Listeria monocytogenes.
Distribution information
Distributed nationwide in the US and also in Canada and Japan
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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