CLASS I Food recall · Reported 15 Apr 2015 · FDA Enforcement Report

garden lites Veggie Chili & Cornbread Melt recalled by classic cooking

classic cooking is recalling garden lites Veggie Chili & Cornbread Melt, distributed nationwide in the US. The recall was initiated on 15 Jan 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes1) LOT # 29914 - EXP DATE 4/26/2016
Quantity recalled96 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1930-2015
FDA event ID
70285
Recalling firm
classic cooking, Jamaica, NY
Classification
Class I
Status
Terminated
Recall initiated
15 Jan 2015
FDA classified
9 Apr 2015
Reported
15 Apr 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Peanuts
Product category
Other

Timeline

15 Jan 2015Recall initiated by company
9 Apr 2015Classified by FDA+84 days
15 Apr 2015Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Cumin contains undeclared peanut protein.

Product as listed by the FDA

garden lites Veggie Chili & Cornbread Melt, Net WT 7 oz (198g). UPC 7-04863-01726-6. KEEP FROZEN.

Where it was distributed

nationwide in retail stores

Nationwide

Questions about this recall

Why was it recalled?

Cumin contains undeclared peanut protein.

Which lots are affected?

1) LOT # 29914 - EXP DATE 4/26/2016

Where was it sold?

nationwide in retail stores

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 70285

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