R.A.B. Food Group LLC Recall: The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk. - F-1542-2018
United States
TerminatedClass II
- Company
- R.A.B. Food Group LLC
- Product
- Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.2…
- Recall date
- March 29, 2018
- Terminated
- September 1, 2021
- Source
- FDA
Reason for recall
The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box, | Not published in this source record | 497 Cases | Lot # 1J026 |
Distribution
- Distribution states MD
- PA
- WA
- CT
- NY
- CO
- CA
- IL
- NJ
- FL
- & MI
- Ontatio Canada.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1542-2018
- Event ID
- 79695
- Status
- Terminated
- Classification
- Class II
- Company
- R.A.B. Food Group LLC
- Product description
- Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box,
- Quantity
- 497 Cases
- Reason
- The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk.
- Recall initiation date
- March 29, 2018
- Report date
- June 20, 2018
- Classification date
- Not published in this source record
- Termination date
- September 1, 2021
- Distribution pattern
- Distribution states MD, PA, WA, CT, NY, CO, CA, IL, NJ, FL, & MI, Ontatio Canada.
- UPC, lot, and code information
- Lot # 1J026
- 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: R.A.B. Food Group LLC
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 |
|---|---|
| Maryland | 1 |
| Pennsylvania | 1 |
| Washington | 1 |
| Connecticut | 1 |
| New York | 1 |
| Colorado | 1 |
| California | 1 |
| Illinois | 1 |
| New Jersey | 1 |
| Florida | 1 |
| Michigan | 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.
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.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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?
FDA classifies this recall as Class II. 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
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How to interpret this historical record
This record is preserved as published by FDA, as of September 1, 2021.
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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