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CriticalFDAfda-F-1133-2017LACERATION

Pheta, cut and packaged in brine, Chapel Hill Creamery, Chapel Hill, NC 27516, sold by 10 lb tub (wholesale) and by individual packages a...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (laceration). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
982
Recall Date
July 27, 2016
Issuing Agency
Hazard
Laceration

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1133-2017.

The products may be contaminated with Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1133-2017.

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 Chapel Hill Creameryllc 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-1133-2017.

Chapel Hill CreameryLLC

FDA

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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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Chapel Hill Creameryllc Recall FAQ

Chapel Hill Creameryllc is the subject of a food safety report: Pheta, cut and packaged in brine, Chapel Hill Creamery, Chapel Hill, NC 27516, sold by 10 lb tub (wholesale) and by individual packages a.... The notice was published on July 27, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 982 units are potentially affected.