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CriticalFDAfda-F-1720-2017LISTERIA

Ruth's Jalapeno Pimento Spread, 12 oz. (UPC 74952-12014), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic con...

⚠ 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.

Category
Units Affected
3,394
Recall Date
February 2, 2017
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1720-2017.

Product has 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-1720-2017.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact B & H Foods Inc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-1720-2017.

B & H Foods Inc

FDA

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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📣 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.

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B & H Foods Inc Recall FAQ

B & H Foods Inc is the subject of a food safety report: Ruth's Jalapeno Pimento Spread, 12 oz. (UPC 74952-12014), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic con.... The notice was published on February 2, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 3,394 units are potentially affected.