CLASS I Food recall · Reported 14 Dec 2016 · FDA Enforcement Report

Willis Eagle Mut Gung Sweetened Ginger recalled by Willis Ocean

Willis Ocean is recalling Willis Eagle Mut Gung Sweetened Ginger, distributed in Florida. The recall was initiated on 26 Aug 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 8935129760691 and no other coding
Quantity recalled30 cases (48 x 7 oz. units per case)

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-0611-2017
FDA event ID
75047
Recalling firm
Willis Ocean, Brooklyn, NY
Classification
Class I
Status
Terminated
Recall initiated
26 Aug 2016
FDA classified
7 Dec 2016
Reported
14 Dec 2016
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Sulfites
Product category
Other

Timeline

26 Aug 2016Recall initiated by company
7 Dec 2016Classified by FDA+103 days
14 Dec 2016Published in enforcement report+7 days

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

Reason for recall

The imported product was found to contain undeclared sulfites

Product as listed by the FDA

Willis Eagle brand MUT GUNG SWEETENED GINGER, NET WEIGHT 200 g (7 oz), UPC 8935129760691

Where it was distributed

Florida

Florida

Questions about this recall

Is Willis Eagle Mut Gung Sweetened Ginger recalled?

Yes. Willis Ocean recalled Willis Eagle Mut Gung Sweetened Ginger on 26 Aug 2016. The recall is Class I and its status is Terminated. Recall number F-0611-2017.

Why was it recalled?

The imported product was found to contain undeclared sulfites

Which lots are affected?

UPC 8935129760691 and no other coding

Where was it sold?

Florida

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.

Other Other recalls

All 4,662