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High RiskFDAfda-F-1850-2018CONTAMINATION

Bow Tie Pasta Caesar Molly's Kitchen, item # 58108.76434, Inner Containter Item # 58108.30168, 2/4.5 # packages per case. UPC 0 58108 3...

Category
Units Affected
121
Recall Date
August 17, 2018
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1850-2018.

Bow Tie Pasta Caesar Molly's Kitchen is recalled due to a potential contamination with Cyclospora. The pasta salad contains spinach that was recalled due to a potential contamination with Cyclospora.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1850-2018.

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 Reser's Fine Foods, 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-1850-2018.

Reser's Fine Foods, Inc.

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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Reser's Fine Foods, Inc. Recall FAQ

Reser's Fine Foods, Inc. is the subject of a produce safety report: Bow Tie Pasta Caesar Molly's Kitchen, item # 58108.76434, Inner Containter Item # 58108.30168, 2/4.5 # packages per case. UPC 0 58108 3.... The notice was published on August 17, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 121 units are potentially affected.