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CriticalFDAfda-F-0614-2024LACERATION

Market Cuts 40 oz Combo Tray Fruit Small 40 Ounce tray UPC 092538001611; (No brand) 80 oz Combo Tray Fruit Large 80 Ounce tray UPC 092538...

⚠ 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
122
Recall Date
November 9, 2023
Issuing Agency
Hazard
Laceration

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0614-2024.

salmonella

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0614-2024.

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 Market Cuts Llc 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-0614-2024.

Market Cuts LLC

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.

How to report to FDAFile a report at FDA

Market Cuts Llc Recall FAQ

Market Cuts Llc is the subject of a produce safety report: Market Cuts 40 oz Combo Tray Fruit Small 40 Ounce tray UPC 092538001611; (No brand) 80 oz Combo Tray Fruit Large 80 Ounce tray UPC 092538.... The notice was published on November 9, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 122 units are potentially affected.