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Leeann Chin, Inc Recall: Sauce found to have a pH higher than specifications.

United States

TerminatedClass III

Company
Leeann Chin, Inc
Product
Lee Ann Chin Thai Peanut Sauce. In glass botle. Net Wt 13…
Recall date
June 22, 2022
Terminated
October 19, 2022
Source
FDA

Reason for recall

Sauce found to have a pH higher than specifications.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Lee Ann Chin Thai Peanut Sauce. In glass botle. Net Wt 13.5 oz (384g) UPC 61248 87100. Shake Well. Refrigerate After Opening. Lee Ann Chin, Bloomington, MN 55431 Not published in this source record 2748 bottles P1 310 22 PEA and P1 013 23 PEA

Distribution

  • MN and WI

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1509-2022
Event ID
90501
Status
Terminated
Classification
Class III
Company
Leeann Chin, Inc
Product description
Lee Ann Chin Thai Peanut Sauce. In glass botle. Net Wt 13.5 oz (384g) UPC 61248 87100. Shake Well. Refrigerate After Opening. Lee Ann Chin, Bloomington, MN 55431
Quantity
2748 bottles
Reason
Sauce found to have a pH higher than specifications.
Recall initiation date
June 22, 2022
Report date
August 3, 2022
Classification date
Not published in this source record
Termination date
October 19, 2022
Distribution pattern
MN and WI
UPC, lot, and code information
P1 310 22 PEA and P1 013 23 PEA
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: Leeann Chin, 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
Minnesota 1
Wisconsin 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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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.