United States
TerminatedClass II
Notification by supplier of a recall of starch ingredient due to metal fragments. Ingredient was used in the manufacture of finished products.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pizza Hut Garlic Dipping Sauce; 144 1.50 oz. cups Net Weight: 13.5 lbs. /6.12 kg Supplier ID: 0005320-01 GSF Product # 01918; Customer Product #: 0072917 Packed exclusively for use by Pizza Hut and its franchisees and licensees. Pizza hut, Plano, TX | Not published in this source record | 2,301 cases | Use by dates: 5/23/2020 |
This recall shares FDA event ID 84682 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
Responsible company: Golden State Foods
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: July 2, 2020Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| District of Columbia | 1 |
| Texas | 1 |
| Kansas | 1 |
| North Carolina | 1 |
| Ohio | 1 |
| Florida | 1 |
| Tennessee | 1 |
| Michigan | 1 |
| Wisconsin | 1 |
| Georgia | 1 |
| Virginia | 1 |
| South Carolina | 1 |
| Kentucky | 1 |
| Illinois | 1 |
| New Jersey | 1 |
| New York | 1 |
| California | 1 |
| Oregon | 1 |
| Colorado | 1 |
| Arizona | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
This record is preserved as published by FDA, as of July 2, 2020.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.
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