CLASS II Food recall · Reported 3 Aug 2016 · FDA Enforcement Report
Ice Nuggets recalled by Kwik Trip
Kwik Trip is recalling Ice Nuggets, distributed in Iowa, Minnesota, Wisconsin. The recall was initiated on 12 Jan 2016 and the FDA has classified it as Class II.
Check your package
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-1835-2016
- FDA event ID
- 73055
- Recalling firm
- Kwik Trip, La Crosse, WI
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 12 Jan 2016
- FDA classified
- 26 Jul 2016
- Reported
- 3 Aug 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Foreign Material
- Product category
- Other
Timeline
| 12 Jan 2016 | Recall initiated by company | |
| 26 Jul 2016 | Classified by FDA | +196 days |
| 3 Aug 2016 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
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
Ice Nuggets, 10 lb plastic bag, UPC 3977919140.
Where it was distributed
WI, IA, MN.
Questions about this recall
Why was it recalled?
Kwik Trip Inc reported a plastic fan broke which lead to pieces of plastic contaminating the ice.
Which lots are affected?
All lots with dates prior to 01/11/16.
Where was it sold?
WI, IA, MN.
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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