Recalls / Class II
Class IIF-0205-2016
Product
Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***Sysco Classic Italian Vegetable Blend***NET WT***2 LB***INGREDIENTS: Zucchini, Carrots, Cauliflower, Italian Green Beans, Baby Lima Beans***UPC 0 74865 01802 9***" Shipping Case UPC Code 10084765018026. Case label reads in part "***Sysco Imperial ITALIAN VEGETABLE BLEND***6/4 lb***INGREDIENTS: Zucchini, Carrots, Cauliflower Florets, Italian Beans, Lima Beans***" No UPC Code on inner generic bag; Shipping Case UPC Code 10074865024447.
- Type
- Food
- Affected lot / code info
- Classic 12/2lb - Item # 74865-01802, lot #'s 29347-4H14D3N, 30525-5A22C3N, 30525-5A22D3N, 30556-5A27D3N, 30734-5B13B3N, 30734-5B13C3N. 30734-5B13D3N, 30982-5C16D3N, 31191-5D09H3N, 31191-5D09J3N, and 31191-5D09K3N with corresponding expiration dates 8/14/2016, 1/22/2017, 1/22/2017, 1/27/2017, 2/13/2017, 2/13/201, 2/13/2017, 3/16/2017, 4/9/2017, 4/9/2017, and 4/9/2017. Imperial 6/4lb - Item # 74865-02444 lot codes 29277-4H10B3N, 30148-4M04B3N, 30605-5B03M3N, 30984-5C16G3N, 31192-5D09K3N, and 31192-5D09L3N with corresponding expiration dates 8/10/2016, 12/4/2016, 2/3/2017 3/16/2017, 4/9/2017, and 4/9/2017.
- Quantity
- Classic 113,712lbs or 4,738cs (12/2lb); Imperial 91,776 lbs or 3,824 cs (6/4lb)
Why it was recalled
Italian Vegetable Blend product is recalled due to potential to be contaminated with Listeria monocytogenes.
Recalling firm
- Firm
- National Frozen Foods Corporation--Seattle
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 1600 Fairview Ave E Floor 2, N/A, Seattle, Washington 98102-3749
Distribution
- Distribution pattern
- distributed nationwide
Timeline
- Recall initiated
- 2015-07-15
- FDA classified
- 2015-11-13
- Posted by FDA
- 2015-11-25
- Terminated
- 2016-01-29
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-0205-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings.