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CriticalFDAfda-F-1174-2022OTHER

POT. RUSSET SLCD W/S 1/16 4/5# (01)10886810715382(10)0016086797 71538 Best if used by: 04/05/22, 04/11/22, 04/15/22, 04/18/22, 04/25/22 I...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
25,433
Recall Date
May 6, 2022
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1174-2022.

Sodium metabisulfite not declared on product label.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1174-2022.

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 Liberty Fruit Co Inc Dba Carol's Cuts 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-1174-2022.

Liberty Fruit Co Inc DBA Carol's Cuts

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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Liberty Fruit Co Inc Dba Carol's Cuts Recall FAQ

Liberty Fruit Co Inc Dba Carol's Cuts is the subject of a food safety report: POT. RUSSET SLCD W/S 1/16 4/5# (01)10886810715382(10)0016086797 71538 Best if used by: 04/05/22, 04/11/22, 04/15/22, 04/18/22, 04/25/22 I.... The notice was published on May 6, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 25,433 units are potentially affected.