CLASS III Food recall · Reported 16 Nov 2016 · FDA Enforcement Report

Original Glazed Doughnuts recalled by Krispy Kreme Doughnut

Krispy Kreme Doughnut is recalling Original Glazed Doughnuts, distributed in Virginia. The recall was initiated on 21 Oct 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesN/A - Product produced on October 20, 2016
Quantity recalled12 ct boxes - 1,672; 6 ct boxes - 985

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0327-2017
FDA event ID
75518
Recalling firm
Krispy Kreme Doughnut, Winston Salem, NC
Classification
Class III
Status
Terminated
Recall initiated
21 Oct 2016
FDA classified
10 Nov 2016
Reported
16 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Cakes & Pastries

Timeline

21 Oct 2016Recall initiated by company
10 Nov 2016Classified by FDA+20 days
16 Nov 2016Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Possible piece of plastic in the product.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Krispy Kreme Doughnuts Original Glazed Doughnuts, 6 count and 12 count boxes.

Where it was distributed

VA

Virginia

Questions about this recall

Why was it recalled?

Possible piece of plastic in the product.

Which lots are affected?

N/A - Product produced on October 20, 2016

Where was it sold?

VA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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