CLASS II Food recall · Reported 14 Nov 2018 · FDA Enforcement Report
Orange plus Citrus Beverage from Concentrate recalled by Campofresco
Campofresco is recalling Orange plus Citrus Beverage from Concentrate. The recall was initiated on 4 Oct 2018 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-0372-2019
- FDA event ID
- 81245
- Recalling firm
- Campofresco, Santa Isabel, PR
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 4 Oct 2018
- FDA classified
- 6 Nov 2018
- Reported
- 14 Nov 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Product category
- Citrus
Timeline
| 4 Oct 2018 | Recall initiated by company | |
| 6 Nov 2018 | Classified by FDA | +33 days |
| 14 Nov 2018 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The product may be contaminated with a sanitizing solution
Product as listed by the FDA
Orange plus Citrus Beverage from Concentrate
Where it was distributed
US Consignees only. No government nor foreign consignees.
Questions about this recall
Is Orange plus Citrus Beverage from Concentrate recalled?
Yes. Campofresco recalled Orange plus Citrus Beverage from Concentrate on 4 Oct 2018. The recall is Class II and its status is Terminated. Recall number F-0372-2019.
Why was it recalled?
The product may be contaminated with a sanitizing solution
Which lots are affected?
Lot 81 14055 T Expiration: Nov 25 18
Where was it sold?
US Consignees only. No government nor foreign consignees.
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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