Tippins 8" Key Lime Pie packaged in aluminum pie plates with plastic covers.
Tippin's Gourmet Pies, LLC recalled this product and the FDA reported the enforcement action on 7 September 2016 as Class II. The recall was initiated by the firm. Product with was manufactured with an ingredient which has the potential to contain low levels of peanut residue.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Tippins 8" Key Lime Pie packaged in aluminum pie plates with plastic covers. The responsible firm listed on the label is TGP, LLC Kansas City, KS 66106. UPC code is 680816050057. Packaged in 8 pies per case. Shipped frozen.
- Reason for recall
- Product with was manufactured with an ingredient which has the potential to contain low levels of peanut residue.
- Recalling firm
- Tippin's Gourmet Pies, LLC
- Firm location
- Kansas City, Kansas, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1991-2016
- Quantity
- 1137 cases of pies
- Distribution
- Recalled product was distributed to Kansas, Missouri, Texas, Oklahoma, Arizona, Wisconsin, and Illinois. There was no government or military distribution.
- Initiated
- 17 June 2016
- Reported by FDA
- 7 September 2016
- Terminated
- 25 April 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot numbers: 04-18-16, 04-21-16, 04-25-16, 04-26-16, 04-27-16, 05-03-16, 05-04-16, 05-05-16, 05-11-16, 05-17-16, and 05-31-2016.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 5 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 5 separate recalls, which almost every published figure does, overstates it by a factor of 5. All 5 of them are listed on this page.
- The recall ran for 10 months, from 17 June 2016 to termination on 25 April 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 3 months after the firm began the recall.
- Recalls of a bakery product run a median of 6 months, so this one was longer than usual for its category. Bakery is overwhelmingly an allergen category rather than a pathogen one: baking is a kill step, but a bakery runs many recipes down shared lines, so the failure that recalls a bakery product is usually a label or a changeover.
Filed under bakery. A product can sit in more than one.
Every product in this recall
The FDA opened 5 enforcement records for this one recall, one per product code. This page carries all of them; the 4 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Other bakery recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Tippin's Gourmet Pies, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 5 records for Tippin's Gourmet Pies, LLC
All 2016 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.