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High RiskFDAfda-F-1151-2022FOREIGN MATERIAL

Dutch Treat Foods Sweet Bacon Bowtie Pasta Salad, 10lbs food service case only, UPC 8-81399-00022-8. Lipari Old Tyme Sweet Bacon Bowtie ...

Category
Units Affected
106
Recall Date
May 20, 2022
Issuing Agency
Hazard
Foreign Material

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1151-2022.

Foreign material (metal). Products contain bacon that is being recalled by Smithfield due to the presence of metal in the bacon.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1151-2022.

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 Craftology, Llc Dba Dutch Treat Foods 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-1151-2022.

Craftology, LLC DBA Dutch Treat Foods

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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Craftology, Llc Dba Dutch Treat Foods Recall FAQ

Craftology, Llc Dba Dutch Treat Foods is the subject of a produce safety report: Dutch Treat Foods Sweet Bacon Bowtie Pasta Salad, 10lbs food service case only, UPC 8-81399-00022-8. Lipari Old Tyme Sweet Bacon Bowtie .... The notice was published on May 20, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 106 units are potentially affected.