Paragon Wholesale Foods, Warrendale, PA 15086 Label: Paragon; Best if used by 10/16/17; Broccoli Florets 1/2 Cup 50/1.7 oz.; X0011932 ...
⚠ 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-0362-2018.
Paragon Wholesale Foods Corp., of Warrendale, PA, is recalling several lots of 1.7 ounce Broccoli Florets in response to a nationwide recall by one of its suppliers, Mann Packing (Salinas, CA) because they have the potential to be contaminated with Listeria monocytogenes
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0362-2018.
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 Paragon Foods 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-0362-2018.
Paragon Foods
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.
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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.
Paragon Foods Recall FAQ
Paragon Foods is the subject of a food safety report: Paragon Wholesale Foods, Warrendale, PA 15086 Label: Paragon; Best if used by 10/16/17; Broccoli Florets 1/2 Cup 50/1.7 oz.; X0011932 .... The notice was published on October 19, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 37 units are potentially affected.