FDA Recall United States TerminatedTerminated: February 13, 2017Historical recordClass I
Atkins Nutritionals, Inc.
- Product
- Blueberry Greek Yogurt Bar 6x5, UPC: 637480025669, Case UPC:…
- Published
- July 27, 2016
- Distribution
- Nationwide
Atkins Nutritionals, Inc. Recall: Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes. - F-1716-2016
United States
TerminatedClass I
- Company
- Atkins Nutritionals, Inc.
- Product
- Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Cas…
- Recall date
- June 3, 2016
- Terminated
- February 13, 2017
- Source
- FDA
Reason for recall
Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Case UPC: 637480059534. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage | 637480055321 | Not published in this source record | Not published in this source record |
Distribution
- Nationwide. Canadian and foreign consignees. No VA/govt/military.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1716-2016
- Status
- Terminated
- Classification
- Class I
- Company
- Atkins Nutritionals, Inc.
- Product description
- Day Break Chocolate Hazelnut Bar 6x5, UPC: 637480055321, Case UPC: 637480059534. Packaging: Outer paper carton containing individually wrapped bars, Ambient Storage
- Quantity
- Not published in this source record
- Reason
- Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes.
- Recall initiation date
- June 3, 2016
- Report date
- July 27, 2016
- Classification date
- Not published in this source record
- Termination date
- February 13, 2017
- Distribution pattern
- Nationwide. Canadian and foreign consignees. No VA/govt/military.
- UPC, lot, and code information
- UPC 637480055321
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Atkins Nutritionals, Inc.
Other recalls from Atkins Nutritionals, Inc.
FDA Recall United States TerminatedTerminated: February 13, 2017Historical recordClass I
Atkins Nutritionals, Inc.
- Product
- Strawberry Almond Bar 6x5, UPC: 637480025904, Case UPC: 6374…
- Published
- July 27, 2016
- Distribution
- Nationwide
FDA Recall United States TerminatedTerminated: February 13, 2017Historical recordClass I
Atkins Nutritionals, Inc.
- Product
- Triple Chocolate Bar 6x5, UPC: 637480035408, Case UPC: 63748…
- Published
- July 27, 2016
- Distribution
- Nationwide
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 |
|---|---|
| Virginia | 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 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 February 13, 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.
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.