CLASS II Food recall · Reported 5 Oct 2016 · FDA Enforcement Report
Triana Family Brioche Donuts Bavarian Cream recalled by Pao De Milho Iii
PAO De Milho III is recalling Triana Family Brioche Donuts Bavarian Cream, distributed in New Jersey. The recall was initiated on 30 Aug 2016 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-2620-2016
- FDA event ID
- 75185
- Recalling firm
- PAO De Milho III, Newark, NJ
- Brand
- Triana
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Aug 2016
- FDA classified
- 28 Sep 2016
- Reported
- 5 Oct 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Cakes & Pastries
Timeline
| 30 Aug 2016 | Recall initiated by company | |
| 28 Sep 2016 | Classified by FDA | +29 days |
| 5 Oct 2016 | 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
Brioche Donuts- Bavarian Cream contain undeclared FD&C yellow #5 and FD&C yellow #6.
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
Triana Family Brioche Donuts Bavarian Cream Net Wt. 0.75 LBS (340 g) 12 -24 Jabez St., Newark, NJ 07106 UPC 000260003995 packaged in a clear plastic clam shell container
Where it was distributed
NJ
Questions about this recall
Why was it recalled?
Brioche Donuts- Bavarian Cream contain undeclared FD&C yellow #5 and FD&C yellow #6.
Which lots are affected?
9/13/2016
Where was it sold?
NJ
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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