Tippin's Gourmet Pies, LLC Recall: Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.

🇺🇸 United States

1. June 17, 2016 - Recall initiated
2. September 7, 2016 - Reported by source
3. April 25, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1993-2016

Status

Terminated

Classification

Class II

Company

Tippin's Gourmet Pies, LLC

Product description

Tippins 9" Keylime Base packaged in ?. UPC code is 680816000205. Packaged in 18 pie bases per case. Shipped frozen. Net wt. 31oz each.

Quantity

Not published in this source record

Reason

Product was manufactured with an ingredient which has the potential to contain low levels of peanut residue.

Recall initiation date

June 17, 2016

Report date

September 7, 2016

Classification date

Not published in this source record

Termination date

April 25, 2017

Distribution pattern

Recalled product was distributed to Kansas, Missouri, Texas, Oklahoma, Arizona, Wisconsin, and Illinois. There was no government or military distribution.

UPC, lot, and code information

Not published in this source record

Voluntary or mandated

Not published in this source record

Initial notification method

Not published in this source record

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: Tippin's Gourmet Pies, LLC

Other recalls from Tippin's Gourmet Pies, LLC

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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