Gertrude Hawk Brands dba Gertrude Hawk Chocolates Recall: Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.

🇺🇸 United States

1. December 13, 2018 - Recall initiated
2. June 26, 2019 - Reported by source
3. June 25, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1465-2019

Event ID

81853

Status

Terminated

Classification

Class II

Company

Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Product description

R.H. Macy & Co. Milk Chocolate Covered Pecan Caramel Clusters, 7oz 1 unit per package, oval metal tin canister, 6 units per case

Quantity

10,848 Units

Reason

Products containing almonds and pecans were distributed in packaging that was mislabeled and did not reveal the presence of almonds and pecans.

Recall initiation date

December 13, 2018

Report date

June 26, 2019

Classification date

Not published in this source record

Termination date

June 25, 2019

Distribution pattern

Product was distributed nationwide, including Hawaii and Guam, in a limited distribution through Macys retail stores and mail order.

UPC, lot, and code information

Lot Codes: 18218463750, 18271463750, 18272463750, 18273463750, 18275463750, 18276463750 All Best Buy Dates; UPC: 7 20227 46375 3

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 81853 with 3 other product entries in Public Health Trace.

Responsible company: Gertrude Hawk Brands dba Gertrude Hawk Chocolates

Other recalls from Gertrude Hawk Brands dba Gertrude Hawk Chocolates

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 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.

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