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High RiskFDAfda-F-0969-2022CONTAMINATION

Thai Noodle Salad Kit 108 oz. bag (behind the counter salad), UPC 0 30223 11270 9, Taylor Farms Southwest, 859 S. 86th Ave, Tolleson, AZ ...

Category
Units Affected
62
Recall Date
March 8, 2022
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0969-2022.

This recall is a result of a supplier recalling an ingredient supplied to us, Thai Noodle Salad. They identified the potential for it to be contaminated with pieces of clear plexiglass.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0969-2022.

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 Taylor Farms Southwest, Inc 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-0969-2022.

Taylor Farms Southwest, Inc

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.

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Taylor Farms Southwest, Inc Recall FAQ

Taylor Farms Southwest, Inc is the subject of a produce safety report: Thai Noodle Salad Kit 108 oz. bag (behind the counter salad), UPC 0 30223 11270 9, Taylor Farms Southwest, 859 S. 86th Ave, Tolleson, AZ .... The notice was published on March 8, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 62 units are potentially affected.