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R & J Almonds, Inc. dba Jonny Almond Nut Co. Recall: R&J Almonds, Inc. dba Jonny Almond Nut Co. initiated a voluntary recall of Salted Caramel Almonds due to undeclared allergen peanuts.

United States

TerminatedClass I

Company
R & J Almonds, Inc. dba Jonny Almond Nut Co.
Product
Salted Caramel Almonds
Recall date
November 7, 2016
Terminated
February 9, 2017
Source
FDA

Reason for recall

R&J Almonds, Inc. dba Jonny Almond Nut Co. initiated a voluntary recall of Salted Caramel Almonds due to undeclared allergen peanuts.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Salted Caramel Almonds Not published in this source record 80 cases 36 lbs/case LOT# 101716 Production Date 10/18/16 Use by date 6/18/17 UPC# 818224010442

Distribution

  • Domestic only- Customer in Michigan Foreign: None VA/DOD: None

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0600-2017
Event ID
75636
Status
Terminated
Classification
Class I
Company
R & J Almonds, Inc. dba Jonny Almond Nut Co.
Product description
Salted Caramel Almonds
Quantity
80 cases 36 lbs/case
Reason
R&J Almonds, Inc. dba Jonny Almond Nut Co. initiated a voluntary recall of Salted Caramel Almonds due to undeclared allergen peanuts.
Recall initiation date
November 7, 2016
Report date
December 14, 2016
Classification date
Not published in this source record
Termination date
February 9, 2017
Distribution pattern
Domestic only- Customer in Michigan Foreign: None VA/DOD: None
UPC, lot, and code information
LOT# 101716 Production Date 10/18/16 Use by date 6/18/17 UPC# 818224010442
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: R & J Almonds, Inc. dba Jonny Almond Nut Co.

Distribution map

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.

Distribution map
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.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

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?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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 instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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