The Crystal Spoon Corp. Recall: Product may be contaminated with E.coli - F-2056-2019
United States
TerminatedClass I
- Company
- The Crystal Spoon Corp.
- Product
- Top Chef Meals Grilled Bison Burger best used by date betwe…
- Recall date
- July 16, 2019
- Terminated
- April 29, 2020
- Source
- FDA
Reason for recall
Product may be contaminated with E.coli
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Top Chef Meals Grilled Bison Burger best used by date between 5/4/19-6/30/19 Unit Size: 6 and 8 oz sizes Container Description: Plastic PETE dual ovenable No specific UPC number | Not published in this source record | 485 | No lot code No serial number |
Distribution
- Nationwide: direct sales to consumers.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2056-2019
- Event ID
- 83347
- Status
- Terminated
- Classification
- Class I
- Company
- The Crystal Spoon Corp.
- Product description
- Top Chef Meals Grilled Bison Burger best used by date between 5/4/19-6/30/19 Unit Size: 6 and 8 oz sizes Container Description: Plastic PETE dual ovenable No specific UPC number
- Quantity
- 485
- Reason
- Product may be contaminated with E.coli
- Recall initiation date
- July 16, 2019
- Report date
- July 31, 2019
- Classification date
- Not published in this source record
- Termination date
- April 29, 2020
- Distribution pattern
- Nationwide: direct sales to consumers.
- UPC, lot, and code information
- No lot code No serial number
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: The Crystal Spoon Corp.
Where this information comes from
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.
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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 I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of April 29, 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.