CLASS I Food recall · Reported 13 Jul 2016 · FDA Enforcement Report

Fried Shrimp Flavoured Fish Bar recalled by Way Fong

Way Fong is recalling Fried Shrimp Flavoured Fish Bar, distributed in New York. The recall was initiated on 16 Mar 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lot numbers beginning with "0" and "8"
Quantity recalled15 cases

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-1629-2016
FDA event ID
73713
Recalling firm
Way Fong, Maspeth, NY
Brand
Fried
Classification
Class I
Status
Terminated
Recall initiated
16 Mar 2016
FDA classified
7 Jul 2016
Reported
13 Jul 2016
Type
Voluntary: Firm initiated
Customers notified by
FAX
Reason category
Undeclared Egg
Product category
Shrimp

Timeline

16 Mar 2016Recall initiated by company
7 Jul 2016Classified by FDA+113 days
13 Jul 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

Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.

Product as listed by the FDA

FRIED SHRIMP FLAVOURED FISH BAR, Net Wt 9.07 Kg 4 X 5 lbs. bulk, Product of Canada, KEEP REFRIGERATED

Where it was distributed

New York

New York

Questions about this recall

Is Fried Shrimp Flavoured Fish Bar recalled?

Yes. Way Fong recalled Fried Shrimp Flavoured Fish Bar on 16 Mar 2016. The recall is Class I and its status is Terminated. Recall number F-1629-2016.

Why was it recalled?

Canadian Food Inspection Agency analytical results revealed the presence of undeclared egg allergen.

Which lots are affected?

All lot numbers beginning with "0" and "8"

Where was it sold?

New York

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

More recalls from Way Fong

All 2
ReportedClassRecallCompanyReasonWhere
FoodCLASS ISeafood Ball Combo Assorti Boulettes Aux Products De Mer recalledSeafood BallWay FongUndeclared EggNY

Other Shrimp recalls

All 145