Recall record at a glance
| Official record | F-1944-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | National Frozen Foods Corporation |
| Report date | Jul 31, 2019 |
| Recall initiation date | Jul 18, 2019 |
| Quantity | 3,124 cases (10/12 oz. bags per case) |
| Location | Albany, OR, United States |
Official product description
Great Value Chopped Spinach, packed in poly bags, net wt. 12 oz. 12 oz. bag UPC: 0 78742 23740 4. master case UPC: 3 00 78742 23740 5. The retail 12 oz. bag label is read in parts: "*** Great Value Chopped Spinach ***INGREDIENTS: SPINACH *** DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716 *** MICROWAVE INSTRUCTIONS: Place frozen, unopened bag with the "this side up" indicator facing up in microwave. Do no pierce bag *** Microwave on high for 6 minutes. During cooking, the bag will slowly inflate. A special vent in the bag will allow the steam to escape and a whistling sound may be heard ***Let stand for 1 minute after cooking. Carefully handle bag at corners and remove from microwave with two hands*** STOVETOP INSTRUCTIONS: Empty frozen contents of bag into a 2-quart nonstick saucepan Add 1 cup water ***Cover and cook over medium heat for 6-7 minutes, stirring occasionally***"
Why the product was recalled
Spinach was recalled due to a potential for contamination with Listeria monocytogenes
Distribution information
Distributed in AL, AR, MO, NE, OK, TX, and WY.
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: E-Mail.
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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