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Ingredients Solutions Inc. Recall: On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food product. The fibers were identified by the recalling firm as 'tie tie' a fibrous rope used for seaweed production that was present in the seaweed ingredient used to manufacture carrageenan. One August 28, 2020 the firm recalled the finished carrageenan.

United States

TerminatedClass II

Company
Ingredients Solutions Inc.
Product
MBF-202 Carrageenan
Recall date
August 27, 2020
Terminated
April 28, 2021
Source
FDA

Reason for recall

On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food product. The fibers were identified by the recalling firm as 'tie tie' a fibrous rope used for seaweed production that was present in the seaweed ingredient used to manufacture carrageenan. One August 28, 2020 the firm recalled the finished carrageenan.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
MBF-202 Carrageenan Not published in this source record 18,000 lbs. 191001-A 191001-B 191002-A Use by dates: 10/01/21 & 10/02/21 191002-B 191003-A

Distribution

  • IA
  • KS
  • WI
  • KY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1435-2020
Event ID
86362
Status
Terminated
Classification
Class II
Company
Ingredients Solutions Inc.
Product description
MBF-202 Carrageenan
Quantity
18,000 lbs.
Reason
On August 28, 2020, the firm's customer discovered colored fibers up to 1/4 " in length after sifting a lot of finished carrageenan intended for use as an ingredient in a finished food product. The fibers were identified by the recalling firm as 'tie tie' a fibrous rope used for seaweed production that was present in the seaweed ingredient used to manufacture carrageenan. One August 28, 2020 the firm recalled the finished carrageenan.
Recall initiation date
August 27, 2020
Report date
September 16, 2020
Classification date
Not published in this source record
Termination date
April 28, 2021
Distribution pattern
IA, KS, WI, KY
UPC, lot, and code information
191001-A 191001-B 191002-A Use by dates: 10/01/21 & 10/02/21 191002-B 191003-A
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: Ingredients Solutions Inc.

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
Iowa 1
Kansas 1
Wisconsin 1
Kentucky 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 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?

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