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High RiskFDAfda-F-1956-2019OTHER

Green Giant Fresh Zucchini Noodles; Fresh Spiralized Zucchini 10.5 oz. (297 g). plastic bag UPC: 605806000881; Item number MSC104102; ...

Category
Units Affected
2,153
Recall Date
June 28, 2019
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1956-2019.

Firm received notification of a positive L. mono test result from a random sample taken from of one our customer's retail locations by the Massachusetts Department of Public Health.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1956-2019.

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 Growers Express S 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-1956-2019.

Growers Express S

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

Growers Express S Recall FAQ

Growers Express S is the subject of a food safety report: Green Giant Fresh Zucchini Noodles; Fresh Spiralized Zucchini 10.5 oz. (297 g). plastic bag UPC: 605806000881; Item number MSC104102; .... The notice was published on June 28, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 2,153 units are potentially affected.