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FDA source record Class II Terminated

Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO Box 514599 LA, CA 90051 Clear plastic bag with front labe...

Recall Date: 2022-12-23 Recalling Firm: World Variety Produce Inc dba Melissa's Record Ref: F-0292-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO Box 514599 LA, CA 90051 Clear plastic bag with front labe... and names World Variety Produce Inc dba Melissa's 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: World Variety Produce Inc dba Melissa's
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2022-12-23
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

Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO Box 514599 LA, CA 90051 Clear plastic bag with front label Package size: 6 count

Reason for Recall / Hazard Identified

Pasta Para Duris was found to contain wheat that is not declared on the label

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

Product was distributed to the states of IL, IN, KY, MI, OH, and WI.

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-0292-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record