Fresh Express, Inc. Recall: Undeclared allergens (milk, wheat, fish (anchovy) and egg. - F-1260-2017
United States
TerminatedClass I
- Company
- Fresh Express, Inc.
- Product
- Fresh Express Hearts of Romaine salad, 9 oz., clear/labeled…
- Recall date
- December 21, 2016
- Terminated
- September 12, 2017
- Source
- FDA
Reason for recall
Undeclared allergens (milk, wheat, fish (anchovy) and egg.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Fresh Express Hearts of Romaine salad, 9 oz., clear/labeled salad bag/ 6 bags per case | Not published in this source record | 100 cases x 6 bags (600/9.oz bags) | Lot # H34711A and H34711B product of USA |
Distribution
- One distributor - Lancaster Foods
- Jessup
- Maryland
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1260-2017
- Event ID
- 76057
- Status
- Terminated
- Classification
- Class I
- Company
- Fresh Express, Inc.
- Product description
- Fresh Express Hearts of Romaine salad, 9 oz., clear/labeled salad bag/ 6 bags per case
- Quantity
- 100 cases x 6 bags (600/9.oz bags)
- Reason
- Undeclared allergens (milk, wheat, fish (anchovy) and egg.
- Recall initiation date
- December 21, 2016
- Report date
- January 25, 2017
- Classification date
- Not published in this source record
- Termination date
- September 12, 2017
- Distribution pattern
- One distributor - Lancaster Foods, Jessup, Maryland
- UPC, lot, and code information
- Lot # H34711A and H34711B product of USA
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Fresh Express, Inc.
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 September 12, 2017.
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.
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