I.Q.F Chopped Spinach, Del Mar Foods Product Corp; 35 lb. Net Weight. brown case fiber with polyliner Del Mar Food Products; Watson...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2235-2017.
Firm was notified by customer of a positive Listeria Monocytogenes result during routine testing upon receipt of IQF frozen chopped spinach supplied by Del Mar Food Products.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2235-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Del Mar Food Products Corp. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2235-2017.
Del Mar Food Products Corp.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Del Mar Food Products Corp. Recall FAQ
Del Mar Food Products Corp. is the subject of a produce safety report: I.Q.F Chopped Spinach, Del Mar Foods Product Corp; 35 lb. Net Weight. brown case fiber with polyliner Del Mar Food Products; Watson.... The notice was published on April 25, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 708 units are potentially affected.