1. WLD HRVST OG2 RED CABBAGE 2. USA/MX OG2 RED CABBAGE 3. USA ORGC GRN CABBAGE 4. WLD HRVST OG2 GRE
Summary
The FDA issued a Class II for 1. WLD HRVST OG2 RED CABBAGE 2. USA/MX OG2 RED CABBAGE 3. USA ORGC GR by UNFI General Corporate. Reason: May be contaminated with fluid from a reach truck.
Details
Source
Food Recall
External ID
H-0234-2025
Action Date
2025-07-16
Status
Terminated
Category
food
Product Description
1. WLD HRVST OG2 RED CABBAGE 2. USA/MX OG2 RED CABBAGE 3. USA ORGC GRN CABBAGE 4. WLD HRVST OG2 GREEN CABBAGE
Lot/Code Info: 1. UPC: 07-11535-51689 case code: 51689 2. UPC: 00-78783-90501 case code: 90501 3. 00-00000-94069 case code: 94069 4. 07-11535-51688 case code: 51688
Quantity Affected: 213 cases (total)
Reason for Recall
May be contaminated with fluid from a reach truck
Distribution
NJ, NY, MD, DC, PA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-07
Company
Providence, RI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 147 food recalls issued in the same week, part of 204 food-related FDA actions this month.
UNFI General Corporate has 31 FDA actions in our database, including 31 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (UNFI General Corporate) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does UNFI General Corporate have FDA actions?
UNFI General Corporate has 31 FDA actions in our database, including 31 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0234-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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