FDA Recall United States Terminated Historical recordClass I
Superior Foods Company
- Product
- Smoked Salmon Spread 5 lb. bulk units; Simply Superior Smo…
- Published
- May 16, 2018
- Distribution
- Domestic only: MI, IN, IL, OH, MN
Superior Foods Company Recall: foreign material (plastic)
United States
TerminatedClass II
- Company
- Superior Foods Company
- Product
- Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in pla…
- Recall date
- July 24, 2025
- Terminated
- September 11, 2025
- Source
- FDA
Reason for recall
foreign material (plastic)
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in plastic tub UPC 4061462440151 | 4061462440151 | 19368 retail units | Lot 16225 Sell by 11-08-25 |
Distribution
- nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0425-2025
- Event ID
- 97352
- Status
- Terminated
- Classification
- Class II
- Company
- Superior Foods Company
- Product description
- Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in plastic tub UPC 4061462440151
- Quantity
- 19368 retail units
- Reason
- foreign material (plastic)
- Recall initiation date
- July 24, 2025
- Report date
- August 20, 2025
- Classification date
- Not published in this source record
- Termination date
- September 11, 2025
- Distribution pattern
- nationwide
- UPC, lot, and code information
- UPC 4061462440151; Lot 16225 Sell by 11-08-25
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Other
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Superior Foods Company
Other recalls from Superior Foods Company
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
