United States
TerminatedClass II
Product is potentially contaminated with Listeria Monocytogenes.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Own Brands , Squash Noodle Medley, 20 Ounces, in a PET Clamshell, UPC 6 88267 18585 4 | Not published in this source record | 1183 units | Lancaster # 2827 Expiration dates of 01/03/21, 01/08/21, 01/11/21, 01/17/21, 01/18/21, and 01/19/21 Code : (0359, 0361, 0362, 0363, 0364, 0365, 0366, 1001, 1002, 1003, 1004, 1005, 1006, 1007, 1008) |
This recall shares FDA event ID 87180 with 7 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
FDA Recall United States TerminatedTerminated: July 27, 2021Historical recordClass II
Responsible company: Lancaster Foods LLC
FDA Recall United States TerminatedTerminated: August 8, 2023Historical recordClass I
FDA Recall United States TerminatedTerminated: August 8, 2023Historical recordClass I
FDA Recall United States TerminatedTerminated: August 8, 2023Historical recordClass I
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 |
|---|---|
| Pennsylvania | 1 |
| Maryland | 1 |
| Massachusetts | 1 |
| Virginia | 1 |
| Delaware | 1 |
| North Carolina | 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.
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This record is preserved as published by FDA, as of July 27, 2021.
Status as reported: Terminated.
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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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