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FDA source record Class I Terminated

Del Monte Apple with Peanut Butter 5.5 oz UPC 717524102393 packaged in clear plastic non flexible container; Del Monte Apples & Peanut Butter dip 6 oz. UPC 717524720979 packaged...

Recall Date: 2022-05-24 Recalling Firm: Del Monte Fresh Produce Company Record Ref: F-1266-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Del Monte Apple with Peanut Butter 5.5 oz UPC 717524102393 packaged in clear plastic non flexible container; Del Monte Apples & Peanut Butter dip 6 oz. UPC 717524720979 packaged... and names Del Monte Fresh Produce Company as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Del Monte Fresh Produce Company
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-05-24
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

Del Monte Apple with Peanut Butter 5.5 oz UPC 717524102393 packaged in clear plastic non flexible container; Del Monte Apples & Peanut Butter dip 6 oz. UPC 717524720979 packaged in clear plastic non flexible container; Get Go Apples with Peanut Butter Dip Net Wt: 5 oz (142g) UPC 0030034937706 packaged in clear plastic non flexible container

Reason for Recall / Hazard Identified

The peanut butter in the snack items have the potential to be contaminated with Salmonella.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

FL, IN, PA, TX and OK

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1266-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record