Kroger (QFC and Fred Meyer) brand, BROCCOLI CAULI MIX KFK, Net wt. 10 oz, UPC8 2676618507 8.…
Recalling firm: Mary's Harvest Fresh Foods, Inc.
Product is recalled due to potential contamination with E.coli O26.
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: Aug 30, 2017.
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826766185078, 826766187515, 887241804235, 887241808349FDA code information
Use by: 8/5/17 8/8/17. Use by: 8/11/17 8/12/17. Use by: 8/9/17 8/10/17.
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Full FDA record and distribution details
Original product description
Kroger (QFC and Fred Meyer) brand, BROCCOLI CAULI MIX KFK, Net wt. 10 oz, UPC8 2676618507 8. Kroger Main & Vine brand, BROCCOLI CAULI MIX, Net wt. 10 oz, UPC 8 2676618751 5. Mary's Harvest brand, Broccoli & Cauliflower, 6/12 oz. packages, UPC 8 8724180834 9. Mary's Harvest brand. Broccoli & Cauliflower mix, 6/16 oz. packages, UPC 8 8724180423 5. INGREDIENTS: Broccoli & Cauliflower
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 826766185078 | Kroger (QFC and Fred Meyer) brand, BROCCOLI CAULI MIX KFK, Net wt. 10 oz, UPC8 2676618507 8. Kroger Main & Vine brand, BROCCOLI CAULI MIX, Net wt. 10 oz, UPC 8 2676618751 5. Mary's Harvest brand, Broccoli |
| UPC | 826766187515 | 76618507 8. Kroger Main & Vine brand, BROCCOLI CAULI MIX, Net wt. 10 oz, UPC 8 2676618751 5. Mary's Harvest brand, Broccoli & Cauliflower, 6/12 oz. packages, UPC 8 8724180834 9. Mary's Harvest brand. Broc |
| UPC | 887241804235 | 9. Mary's Harvest brand. Broccoli & Cauliflower mix, 6/16 oz. packages, UPC 8 8724180423 5. INGREDIENTS: Broccoli & Cauliflower |
| UPC | 887241808349 | 751 5. Mary's Harvest brand, Broccoli & Cauliflower, 6/12 oz. packages, UPC 8 8724180834 9. Mary's Harvest brand. Broccoli & Cauliflower mix, 6/16 oz. packages, UPC 8 8724180423 5. INGREDIENTS: Broccoli |
Original FDA recall reason
Product is recalled due to potential contamination with E.coli O26.
Recall details
- Recall number
- F-3417-2017
- Event ID
- 77893
- FDA status
- Terminated
- Initiated
- Aug 3, 2017
- Reported
- Aug 30, 2017
- Classified
- Aug 22, 2017
- Terminated
- Aug 30, 2017
- Quantity
- 713/10 oz. packages; 3 cases (6/12 oz. packages); 3 cases (6/16 oz. packages)
- Location
- Portland, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
distributed in OR and WA
Data updated September 16, 2026. View official FDA data ↗
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