Skip to main content
CriticalFDAfda-F-2585-2015LISTERIA

Blue Bell Ice Cream Strawberry Still a 1/2 Gal (2 QTS)

⚠ 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
3,075,027
Recall Date
March 13, 2015
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2585-2015.

Five patients who were treated in a single hospital in Kansas were infected with one of four rare strains of Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2585-2015.

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 Blue Bell Creameries, L.p. 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-2585-2015.

Blue Bell Creameries, L.P.

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.

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.

How to report to FDAFile a report at FDA

Blue Bell Creameries, L.p. Recall FAQ

Blue Bell Creameries, L.p. is the subject of a dairy safety report: Blue Bell Ice Cream Strawberry Still a 1/2 Gal (2 QTS). The notice was published on March 13, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 3,075,027 units are potentially affected.