Linden Cookies, Inc Recall: The product contains undeclared milk from the bulk chocolate chips received from the supplier.

🇺🇸 United States

1. December 13, 2016 - Recall initiated
2. January 18, 2017 - Reported by source
3. August 17, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1222-2017

Event ID

75931

Status

Terminated

Classification

Class I

Company

Linden Cookies, Inc

Product description

Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ., UPC 76809-30017; b) Chocolate Chippers (Mini), NET WT 1.1 OZ., UPC 76809-30090; c) 3 LARGE CHOCOLATE CHIP COOKIES (Pack), NET WT. 1.75 OZ. UPC 76809-30010 --- LINDEN COOKIES, INC. 25 BRENNER DRIVE CONGERS, NY 10920

Quantity

2 oz.: 864,810 packages; 1.1 oz.: 962,316 packages

Reason

The product contains undeclared milk from the bulk chocolate chips received from the supplier.

Recall initiation date

December 13, 2016

Report date

January 18, 2017

Classification date

Not published in this source record

Termination date

August 17, 2017

Distribution pattern

Florida, Virginia, Maryland, Delaware, New Jersey, New York, Connecticut, and Massachusetts

UPC, lot, and code information

UPC 76809-30017; a): Sell By Dates Feb. 8, 2017 through March 28, 2017; b): Sell By Dates Feb. 8, 2017 through March 28, 2017; c): Dec. 14, 2016 through Feb 01, 2017

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Linden Cookies, 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: July 18, 2026 ET

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.

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.

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