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Fishtrap Dairy LLC Recall: Inhibitory substance was detected.

United States

TerminatedClass II

Company
Fishtrap Dairy LLC
Product
Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.2…
Recall date
November 19, 2021
Terminated
January 25, 2022
Source
FDA

Reason for recall

Inhibitory substance was detected.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 16 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00117 0. Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 32 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00116 3. Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 64 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00123 1. The Ingredients statement on the label is read in part "*** MILK, SUGAR, COCOA, CORNSTARCH, SALT, CARRAGEENAN, GUAR GUM, & VANILLIN***". Not published in this source record Chocolate milk = 216/64 oz. bottles; 679/32 oz. bottles; 983/16 oz. bottles Best by 12/05/21 B. Plant # 53-05.

Distribution

  • distributed directly in WA.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0349-2022
Event ID
89099
Status
Terminated
Classification
Class II
Company
Fishtrap Dairy LLC
Product description
Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 16 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00117 0. Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 32 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00116 3. Twin Brook Creamery brand, Pasteurized Chocolate Milk, > 3.25 % fat, packaged in 64 oz. glass bottle with a brown cap, Refrigerated. UPC 8 97605 00123 1. The Ingredients statement on the label is read in part "*** MILK, SUGAR, COCOA, CORNSTARCH, SALT, CARRAGEENAN, GUAR GUM, & VANILLIN***".
Quantity
Chocolate milk = 216/64 oz. bottles; 679/32 oz. bottles; 983/16 oz. bottles
Reason
Inhibitory substance was detected.
Recall initiation date
November 19, 2021
Report date
December 29, 2021
Classification date
Not published in this source record
Termination date
January 25, 2022
Distribution pattern
distributed directly in WA.
UPC, lot, and code information
Best by 12/05/21 B. Plant # 53-05.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 89099 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Fishtrap Dairy LLC

Product
Twin Brook Creamery brand, Pasteurized 1% Milk, Vit D3 Vit…
Published
December 29, 2021
Distribution
distributed directly in WA.

View recall →

Responsible company: Fishtrap Dairy LLC

Other recalls from Fishtrap Dairy LLC

FDA Recall United States Terminated Historical recordClass II

Fishtrap Dairy LLC

Product
Twin Brook Creamery brand, Pasteurized 1% Milk, Vit D3 Vit…
Published
December 29, 2021
Distribution
distributed directly in WA.

View recall →

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
Washington 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?

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.