CLASS II Food recall · Reported 6 May 2015 · FDA Enforcement Report

Sunrise Foods Saffron (Kasvbha) recalled by Phil-Am Trading

Phil-Am Trading is recalling Sunrise Foods Saffron (Kasvbha), distributed in New Jersey, New York. The recall was initiated on 11 Mar 2015 and the FDA has classified it as Class II.

Recall details

Recall number
F-2032-2015
FDA event ID
70790
Recalling firm
Phil-Am Trading, Jersey City, NJ
Brand
Sunrise
Classification
Class II
Status
Terminated
Recall initiated
11 Mar 2015
FDA classified
24 Apr 2015
Reported
6 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Other

Timeline

11 Mar 2015Recall initiated by company
24 Apr 2015Classified by FDA+44 days
6 May 2015Published in enforcement report+12 days

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

Reason for recall

Product contains unallowable dyes: 16255 - Ponceau 4R (E124 - Acid Red 18 and 15510 - Orange II - Acid Orange 7; and undeclared FD&C Yellow #5.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Sunrise Foods Saffron (Kasvbha), Net Wt. 1 oz. (29g), Product of the Philippines, Manufactured by: Sunrise Native Foods Product, GMC May-Tamo Bagungbayan Teresa, Rizal, Philippines

Where it was distributed

NJ and NY

New JerseyNew York

Questions about this recall

Why was it recalled?

Product contains unallowable dyes: 16255 - Ponceau 4R (E124 - Acid Red 18 and 15510 - Orange II - Acid Orange 7; and undeclared FD&C Yellow #5.

Where was it sold?

NJ and NY

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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