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CriticalFDAfda-F-2821-2017LISTERIA

Cape Cod Cranberry Trail Mix; 25 lbs. bulk containers; cardboard box; expiration date 11/18/17.

⚠ 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.

Brand
Category
Units Affected
93
Recall Date
June 16, 2017
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2821-2017.

The firm was notified that the date vendor had a positive test for Listeria in the vendor' s facility. Dates are an ingredient in the product. HMS Host is initiating a precautionary voluntary recall.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2821-2017.

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 Hmshost 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-2821-2017.

Hmshost

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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Hmshost Recall FAQ

Hmshost is the subject of a produce safety report: Cape Cod Cranberry Trail Mix; 25 lbs. bulk containers; cardboard box; expiration date 11/18/17.. The notice was published on June 16, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 93 units are potentially affected.