CLASS II Food recall · Reported 23 Aug 2017 · FDA Enforcement Report
FPI 1/10.35 Fiesta Style Stuffed Alaska Pollock Portions recalled
High Liner Foods is recalling FPI 1/10.35 Fiesta Style Stuffed Alaska Pollock Portions, distributed nationwide in the US. The recall was initiated on 9 Jun 2017 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-2694-2017
- FDA event ID
- 77489
- Recalling firm
- High Liner Foods, Portsmouth, NH
- Brand
- Fpi
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Jun 2017
- FDA classified
- 15 Aug 2017
- Reported
- 23 Aug 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Milk
- Product category
- Other
Timeline
| 9 Jun 2017 | Recall initiated by company | |
| 15 Aug 2017 | Classified by FDA | +67 days |
| 23 Aug 2017 | 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
Product may contain undeclared milk.
Product as listed by the FDA
FPI 1/10.35 Fiesta Style Stuffed Alaska Pollock Portions 3.6 oz.., Item Number: 06436
Where it was distributed
Nationwide
Questions about this recall
Is FPI 1/10.35 Fiesta Style Stuffed Alaska Pollock Portions recalled?
Yes. High Liner Foods recalled FPI 1/10.35 Fiesta Style Stuffed Alaska Pollock Portions on 9 Jun 2017. The recall is Class II and its status is Terminated. Recall number F-2694-2017.
Why was it recalled?
Product may contain undeclared milk.
Which lots are affected?
Lot Number: 0046323197; 0047026190;
Where was it sold?
Nationwide
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 21 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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