ZENSHI HANDCRAFTED SUSHI Chef Sampler A#3 (Crunchy, Rainbow, Chili) 15pc Net Wt.
Harris Teeter recalled this product and the FDA reported the enforcement action on 9 July 2025 as Class I. The recall was initiated by the firm. Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- ZENSHI HANDCRAFTED SUSHI Chef Sampler A#3 (Crunchy, Rainbow, Chili) 15pc Net Wt. 14.8oz (420g) UPC 0 23012 94331 8
- UPC
- 023012943318
- Reason for recall
- Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Recalling firm
- Harris Teeter
- Firm location
- Matthews, North Carolina, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- H-0126-2025
- Quantity
- 3,912 trays
- Distribution
- Product was shipped to the following states: DC, DE, FL, GA, MD, NC, SC & VA.
- Initiated
- 20 May 2025
- Reported by FDA
- 9 July 2025
- Terminated
- 24 July 2025
- Firm notified by
- Letter
- Product codes
- All lots
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 83 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 83 separate recalls, which almost every published figure does, overstates it by a factor of 83. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 83 of them.
- The recall ran for 2 months, from 20 May 2025 to termination on 24 July 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 5 states, and the FDA published the enforcement report 7 weeks after the firm began the recall.
- Recalls of a prepared meal or sandwich run a median of 6 months, so this one was shorter than usual for its category. Prepared meals concentrate every other category's hazards into one package: they are assembled from many components, handled after any cook step, sold ready to eat, and carry an ingredient list long enough to lose an allergen in.
Named in the distribution pattern: Delaware, Florida, Georgia, Maryland, North Carolina. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Salmonella
Salmonella is a bacterium that survives in low-moisture foods for months, which is why it appears in recalls of products that carry no water for it to grow in: nut butters, spices, flour and dry pet food.
A preventive controls plan covers Salmonella contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(1)
- Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
- 21 CFR 117.165(a)(2)
- Product testing: testing as a verification activity, appropriate to the facility, the food and the nature of the preventive control.
Filed under prepared meals and sandwiches. A product can sit in more than one.
Other prepared meals and sandwiches recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Harris Teeter
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 92 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-10-15 | Harris Teeter ASIAGO TEXAS TOAST, NET WT 5.0OZ (0.3lb), INGREDIENTS BREAD***CONTAINS WHEAT, UPC 0 72036 95364 3, Harris Teeter Raleigh, NC | Harris Teeter | Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in the contain statement. | Class I |
| 2025-10-15 | Harris Teeter CINNAMON TEXAS TOAST, NET WT 5.0oz (0.31g), INGREDIENTS BREAD*** CONTAINS WHEAT, UPC 0 72036 95734 4, Harris Teeter Raleigh, NC | Harris Teeter | Undeclared Milk. During production the firm discovered that the ingredients "cheese and butter" is not listed in the ingredient statement and therefore the allergen milk was not listed in the contain statement. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Hybrid Ichi Platter 30pc Net Wt. 27.6oz UPC 0 23012 94256 4 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Ultimate Chili Roll - Salmon 10pc Net Wt. 10.4oz UPC 0 23012 94326 4 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Duo Combo - CA Salad & Rainbow Roll 10pc Net Wt 8.1oz UPC 0 23012 94205 2 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Duo Combo - Salmon Avocado & Rainbow Roll 10pc Net Wt 7.9oz UPC 0 23012 94207 6 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll 10pc (Brown Rice) Net Wt 8.1oz UPC 0 23012 94284 7 & UPC 0 23012 95143 6 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Grilled Salmon Roll Net Wt. 8.6oz UPC 0 23012 94217 5 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Shrimp 10pc Net Wt 10.0oz UPC 0 23012 95042 2 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
| 2025-07-09 | ZENSHI HANDCRAFTED SUSHI Hawaiian Roll - Tuna 10pc Net Wt. 11.6oz UPC 0 23012 94369 1 | Harris Teeter | Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi. | Class I |
All 93 records for Harris Teeter
All 2025 recalls · All FDA food recall data
21 CFR 117.135(c)(1) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.