CLASS II Food recall · Reported 9 Nov 2016 · FDA Enforcement Report
Nu-Quench Lime Bar Mix recalled by Beverage International
Beverage International is recalling Nu-Quench Lime Bar Mix, distributed in Texas. The recall was initiated on 30 Sep 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-0382-2017
- FDA event ID
- 75352
- Recalling firm
- Beverage International, Pasadena, TX
- Brand
- Nu-Quench
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 30 Sep 2016
- FDA classified
- 2 Nov 2016
- Reported
- 9 Nov 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Citrus
Timeline
| 30 Sep 2016 | Recall initiated by company | |
| 2 Nov 2016 | Classified by FDA | +33 days |
| 9 Nov 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
Undeclared Yellow #5 in product.
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
Nu-Quench Lime Bar Mix 32 Oz. packaged in plastic bottle, 12 bottles per case
Where it was distributed
TX
Questions about this recall
Is Nu-Quench Lime Bar Mix recalled?
Yes. Beverage International recalled Nu-Quench Lime Bar Mix on 30 Sep 2016. The recall is Class II and its status is Terminated. Recall number F-0382-2017.
Why was it recalled?
Undeclared Yellow #5 in product.
Which lots are affected?
Bar Code# UPC638845774734
Where was it sold?
TX
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 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.
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