Recalls / Class I
Class IF-1646-2016
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Dr. Praeger's California Veggie Burgers, 26 x 10 oz./box, Best if used by: May-18-2018, UPC 0 80868 00010, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
- Type
- Food
- Affected lot / code info
- Lot #F16BI-01A VB26 Case code: N16CH-01B Retail unit code: N16CH Best by: 1/27/2018 Case code: T16AD-01B Retail unit code: T16AD Best by: 2/03/2018 Case code: T16AJ-02A Retail unit code: T16AJ Best by: 2/09/2018 Case code: T16BI-02B Retail unit code: T16BI Best by: 2/18/2018 Case code: T16BI-02D Retail unit code: T16BI Best by: 2/18/2018 Case code: T16CD-02B Retail unit code: T16CD Best by: 2/23/2018 Case code: T16CE-03A Retail unit code: T16CE Best by: 2/24/2018 Case code: H16AI-04B Retail unit code: H16AI Best by: 3/08/2018 Case code: H16AJ-01A Retail unit code: H16AJ Best by: 3/09/2018 Case code: H16BG-02A Retail unit code: H16BG Best by: 3/16/2018 Case code: H16BG-02N Retail unit code: H16BG Best by: 3/16/2018 Case code: H16DA-01A Retail unit code: H16DA Best by: 3/30/2018 Case code: R16AH-01A Retail unit code: R16AH Best by: 4/07/2018 Case code: R16BD-01B Retail unit code: R16BD Best by: 4/13/2018
- Quantity
- 9,679 cases
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.
Recalling firm
- Firm
- Dr. Praeger'S Sensible Foods
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 9 Boumar Pl, Elmwood Park, New Jersey 07407-2615
Distribution
- Distribution pattern
- US Nationwide and Foreign
Timeline
- Recall initiated
- 2016-05-13
- FDA classified
- 2016-07-08
- Posted by FDA
- 2016-07-20
- Terminated
- 2017-10-04
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1646-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings.