When Was Lavoi Corporation d/b/a/ Epi De France Last Recalled?
Lavoi Corporation d/b/a/ Epi De France was last involved in an FDA food recall on 2015-02-24. Its first recorded recall was on 2015-02-24, spanning 4 recalls in total. All of its recalls have since been classified as completed or terminated by the FDA.
Lavoi Corporation d/b/a/ Epi De France Recall Timeline
| Milestone | Date / Value |
|---|---|
| Most recent recall | 2015-02-24 |
| First recorded recall | 2015-02-24 |
| Total recalls on record | 4 |
| Active (ongoing) recalls | 0 |
Recall Severity Breakdown
| Metric | Value |
|---|---|
| Total Recalls | 4 |
| Class I (Dangerous) | 0 |
| Class II (Moderate) | 4 |
| Class III (Low Risk) | 0 |
| Active Recalls | 0 |
| Most Recent | 2015-02-24 |
Frequently Asked Questions
When was Lavoi Corporation d/b/a/ Epi De France last recalled?
The most recent FDA recall involving Lavoi Corporation d/b/a/ Epi De France was issued on 2015-02-24. Its earliest recorded recall was on 2015-02-24, and it has 4 FDA recalls on record overall.
Does Lavoi Corporation d/b/a/ Epi De France have any active recalls?
No. None of Lavoi Corporation d/b/a/ Epi De France's FDA recalls are currently marked Ongoing — all have been classified as completed or terminated.
How serious have Lavoi Corporation d/b/a/ Epi De France's recalls been?
Of Lavoi Corporation d/b/a/ Epi De France's 4 FDA recalls, 0 were Class I (a reasonable probability of serious health consequences or death), 4 Class II (possible temporary or reversible health effects), and 0 Class III (unlikely to cause adverse health effects).
Is Lavoi Corporation d/b/a/ Epi De France safe?
Lavoi Corporation d/b/a/ Epi De France has had 4 FDA food recalls, including 0 Class I (most serious) recalls. The most recent recall was on 2015-02-24.
More about Lavoi Corporation d/b/a/ Epi De France
Lavoi Corporation d/b/a/ Epi De France was last involved in an FDA food recall on 2015-02-24. Its first recorded recall was on 2015-02-24, spanning 4 recalls in total. All of its recalls have since been classified as completed or terminated by the FDA.
The data source behind this answer is the FDA openFDA enforcement-report API. Every figure on the page traces back to that source; the methodology page describes the inputs and the refresh cadence in full detail.
For readers turning this answer into action: cross-reference against the underlying the FDA openFDA enforcement-report API record before acting on time-sensitive decisions. The site renders the data as it was published; subsequent revisions can shift the picture, and the live federal data is always the authoritative current reference.
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.