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Schwan's Global Supply Chain, Inc. Recall: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is being due to potential glass contamination.

United States

TerminatedClass II

Company
Schwan's Global Supply Chain, Inc.
Product
Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56…
Recall date
November 8, 2018
Terminated
July 17, 2019
Source
FDA

Reason for recall

One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is being due to potential glass contamination.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz. Not published in this source record 2000 cases (12 containers per case) Product code date that begins with "188211". The code can be found next to the large 206 on bottom of carton

Distribution

  • nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0703-2019
Event ID
81533
Status
Terminated
Classification
Class II
Company
Schwan's Global Supply Chain, Inc.
Product description
Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz.
Quantity
2000 cases (12 containers per case)
Reason
One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is being due to potential glass contamination.
Recall initiation date
November 8, 2018
Report date
December 19, 2018
Classification date
Not published in this source record
Termination date
July 17, 2019
Distribution pattern
nationwide
UPC, lot, and code information
Product code date that begins with "188211". The code can be found next to the large 206 on bottom of carton
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Schwan's Global Supply Chain, Inc.

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.

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.