Drug recall
El Campestre Brand Camaron Aquachile. Packaged in 2/5lbs white plastic buckets with lid and handle, into…
FDA recall event 65499 · Class I, Class II, Class III · El Campestre
Key facts
| Event ID | 65499 |
|---|---|
| Recall numbers | F-1760-2013, F-1761-2013, F-1762-2013, F-1763-2013, F-1764-2013, F-1765-2013 |
| Recalling firm | El Campestre |
| Product type | Food |
| Products | El Campestre Brand Camaron Aquachile. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"EL CAMPESTRE CAMARON AGUACHILE***NET WT.10…, El Campestre Brand Ceviche De Basa. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"EL CAMPESTRE CEVICHE DE BASA***NET WT.10…, El Campestre Brand Ceviche De Camaron. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"EL CAMPESTRE CEVICHE DE CAMARON***NET WT.10…, El Campestre Brand Ceviche Mixto, 2/5 lbs bulk containers into 1/10lbs carton. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"CEVICHE…, El Campestre Brand Ceviche Mixto De Basa. Packaged in 2/5lbs white plastic buckets with lid and handle, into 1/10lbs carton. Labeling reads in part:"EL CAMPESTRE CEVICHE MIXTO DE BASA***NET WT.10… and 1 more |
| Classification | Class I, Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | El Campestre initiated this recall due to the following reason: mislabeling: does not contain Basa fish, it contains Swai fish., El Campestre initiated this recall due to the following reason: mislabeling: Shrimp not listed in English, but the whole shrimp are visible., El Campestre initiated this recall due to the following reason: shrimp are not listed in English, but the whole shrimp are… |
| Initiation date | Jun 13, 2013 |
| Report date | Aug 7, 2013 |
| Termination date | Aug 20, 2013 |
| City | Compton |
| State | CA |
| Country | United States |
| FEI number | 3010233543 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: