HEB brand Broccoli & Cauliflower
Recalling firm: Mann Packing Company, Inc.
Why it was recalled
CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.
The exact product
HEB brand Broccoli & Cauliflower; UPC: 41220975037; Mann Brand Broccoli & Cauliflower: UPC: 10716519010054; 12 oz. UPC: 716519013034 - US and Canada Marketside brand Broccoli & Cauliflower; 12 oz. UPC: 681131328852; Signature Farms brand Broccoli & Cauliflower: 12 oz. UPC 21130983384; 28 oz. UPC: 21130984497; 12 oz. UPC: 716519013034 - US And Canada
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Best If Enjoyed By date of October 11, 2019 to November 16, 2019
| Type | Code / value | Context |
|---|---|---|
| UPC | 681131328852 | 13034 - US and Canada Marketside brand Broccoli & Cauliflower; 12 oz. UPC: 681131328852; Signature Farms brand Broccoli & Cauliflower: 12 oz. UPC 21130983384; 28 oz. UPC: 21130984497; 12 oz. UPC: 7 |
| UPC | 716519013034 | 75037; Mann Brand Broccoli & Cauliflower: UPC: 10716519010054; 12 oz. UPC: 716519013034 - US and Canada Marketside brand Broccoli & Cauliflower; 12 oz. UPC: 681131328852; Signature Farms brand Br |
| UPC | 716519013034 | & Cauliflower: 12 oz. UPC 21130983384; 28 oz. UPC: 21130984497; 12 oz. UPC: 716519013034 - US And Canada |
Recall details
- Recall number
- F-0249-2020
- Event ID
- 84190
- FDA status
- Terminated
- Initiated
- Nov 3, 2019
- Reported
- Nov 27, 2019
- Classified
- Dec 10, 2019
- Terminated
- Apr 6, 2023
- Quantity
- Total: 1,286,466 cases - US,. 141,030 cartons Canada
- Location
- Salinas, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
US and Canada and Japan
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.