FDA recall record

Gardner Pie Company Product is a 32-ounce Key Lime pie sold at the firm's retail recall — FDA F-2244-2016

The firm was notified by their supplier of graham cracker crumbs that the flour used to manufacture the crumbs was potentially contaminated with peanut…

Class IIclassification
F-2244-2016official record ID
Sep 21, 2016report date

Recall record at a glance

Official recordF-2244-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGardner Pie Company
Report dateSep 21, 2016
Recall initiation dateJun 17, 2016
Quantity163 individual pies
LocationAkron, OH, United States

Official product description

Product is a 32-ounce Key Lime pie sold at the firm's retail outlet only. Pie is packed in a cardboard carton with an aluminum pie pan and a plastic dome lid. Retail pie is not labeled. Customers are provided the flavor of pie they select for purchase.

Why the product was recalled

The firm was notified by their supplier of graham cracker crumbs that the flour used to manufacture the crumbs was potentially contaminated with peanut residue. The graham cracker crumbs are used in the production of key lime pie, and cheesecake. The crumbs are used to make the bottom crust of pie and cheesecake.

Distribution information

The state of Ohio only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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