Class IITerminatedVoluntary: Firm initiated
HEB: food recall F-0628-2025
HEB of San Antonio, TX recalled " Spinach Artichoke Dip (Sold Hot) 1 lb " Spinach Artichoke Dip (Sold Cold) 1 lb " Spinach Artichoke Dip (Sold in Bulk… Reason: Potential metal inclusion. The FDA listed it as Class II in its Enforcement Report dated Mar 19, 2025; distribution: Texas.
Record status as published: Terminated (terminated Feb 10, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- " Spinach Artichoke Dip (Sold Hot) 1 lb " Spinach Artichoke Dip (Sold Cold) 1 lb " Spinach Artichoke Dip (Sold in Bulk for Customer Self Service)
- Product quantity
- 45lbs
- Reason for recall
- Potential metal inclusion
- Codes, lots and dates on the package
- Spinach Artichoke Dip Sold Hot 200000509996 Packed on 02.09.25 Spinach Artichoke Dip Sold Cold 29618800000 Packed on 02.09.25 Spinach Artichoke Dip Sold in Bulk for Customer Self Service Item Code 296188 Packed on 02.09.25
- Distribution pattern
- Texas
- Recalling firm
- HEB, San Antonio, TX
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Press Release
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Feb 9, 2025 |
| Classified by the FDA | Mar 13, 2025 |
| Published in the Enforcement Report | Mar 19, 2025 |
| Terminated | Feb 10, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0628-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.