Class ITerminated in FDA datasetRecall initiated May 13, 2016

Aldi Kale Burger, Net 18.75 lbs, 30 x 10 oz (284 grams), Sell By: May -17-2018

Recalling firm: Dr. Praeger'S Sensible Foods

Why it was recalled

Dr. Praeger's Sensible Food/Ungar's Food Products is voluntarily recalling various not-ready-to eat frozen products because they may be contaminated with Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 4, 2017.

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ProductAldi Kale Burger, Net 18.75 lbs, 30 x 10 oz (284 grams), Sell By: May -17-2018
Package size18.75 lbs

FDA code information

Item #50206 AL-50206-R30 Case code: H16AH-02A Retail unit code: H16AH Best by: 3/07/2018 Case code: H16AH-02B Retail unit code: H16AH Best by: 3/07/2018 Case code: H16CC-01A Retail unit code: H16CC Best by: 3/22/2018

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Full FDA record and distribution details

Original product description

Aldi Kale Burger, Net 18.75 lbs, 30 x 10 oz (284 grams), Sell By: May -17-2018

Extracted codes and context

TypeCode / valueContext
best by3/07/2018m #50206 AL-50206-R30 Case code: H16AH-02A Retail unit code: H16AH Best by: 3/07/2018 Case code: H16AH-02B Retail unit code: H16AH Best by: 3/07/2018 Case code: H16CC-01A Retail unit code: H16CC Best by:
best by3/07/2018H16AH Best by: 3/07/2018 Case code: H16AH-02B Retail unit code: H16AH Best by: 3/07/2018 Case code: H16CC-01A Retail unit code: H16CC Best by: 3/22/2018
best by3/22/2018H16AH Best by: 3/07/2018 Case code: H16CC-01A Retail unit code: H16CC Best by: 3/22/2018

Original FDA recall reason

Dr. Praeger's Sensible Food/Ungar's Food Products is voluntarily recalling various not-ready-to eat frozen products because they may be contaminated with Listeria monocytogenes.

Recall details

Recall number
F-1634-2016
Event ID
74182
FDA status
Terminated
Initiated
May 13, 2016
Reported
Jul 20, 2016
Classified
Jul 8, 2016
Terminated
Oct 4, 2017
Quantity
1,871 cases
Location
Elmwood Park, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US Nationwide and Foreign

FDA source record · F-1634-2016

Data updated September 16, 2026. View official FDA data ↗

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