CLASS II Food recall · Reported 21 Aug 2013 · FDA Enforcement Report
"***Gasco Golden Egg Yellow Shade Liquid***" & drums recalled
Gasco Industrial is recalling "***Gasco Golden Egg Yellow Shade Liquid***" & drums, distributed in Puerto Rico. The recall was initiated on 8 Jul 2013 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-1808-2013
- FDA event ID
- 65700
- Recalling firm
- Gasco Industrial, Gurabo, PR
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Jul 2013
- FDA classified
- 14 Aug 2013
- Reported
- 21 Aug 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Allergens
- Product category
- Eggs
Timeline
| 8 Jul 2013 | Recall initiated by company | |
| 14 Aug 2013 | Classified by FDA | +37 days |
| 21 Aug 2013 | Published 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
Undeclared allergens: 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
"***Gasco Golden Egg Yellow Shade Liquid***" 32 oz plastic bottles & 15 gallon drums
Where it was distributed
Puerto Rico only
Questions about this recall
Why was it recalled?
Undeclared allergens: Yellow #5
Which lots are affected?
080812, 110912, 051112, 220413
Where was it sold?
Puerto Rico only
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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