Recall record at a glance
| Official record | F-1913-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Coastal Green Vegetable Company, LLC |
| Report date | Apr 15, 2015 |
| Recall initiation date | Mar 20, 2015 |
| Quantity | N/A |
| Location | Oxnard, CA, United States |
Official product description
-Frozen IQF Conventional Chopped Spinach Packed in Bulk in 1,000 lb tote bins or 40 lb cases Each case and/or tote bin is tagged with a label containing the following information, item number, lot code, production date, weight, and SKU number. 00SP0241T10 Organic Spinach Cut Leaf Lot # 1431930067 Quantity: 1 Net Weight: 1,000 lbs Prod Date 11/15/2014 Product of USA Coastal Green Vegetable Co., LLC Oxnard, CA 93030 Prod Date 11/15/2014 1,000.00 lbs 1431930067 X0SPO241110 Organic Spinach Cut Leaf
Why the product was recalled
This recall is being initiated due to test results that show the presence of Listeria monocytogenes in product that was shipped erroneously. Other finished product test results show the presence of Listeria but was not speciated, and out precaution those lots are also included in this recall. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in you
Distribution information
The firm has customers located in the U.S. only in the following states; CA, OR, WA, and WI.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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