When Was Aurora Products, INC. Last Recalled?
Aurora Products, INC. was last involved in an FDA food recall on 2017-11-01. Its first recorded recall was on 2015-03-20, spanning 6 recalls in total. All of its recalls have since been classified as completed or terminated by the FDA.
Aurora Products, INC. Recall Timeline
| Milestone | Date / Value |
|---|---|
| Most recent recall | 2017-11-01 |
| First recorded recall | 2015-03-20 |
| Total recalls on record | 6 |
| Active (ongoing) recalls | 0 |
Recall Severity Breakdown
| Metric | Value |
|---|---|
| Total Recalls | 6 |
| Class I (Dangerous) | 4 |
| Class II (Moderate) | 2 |
| Class III (Low Risk) | 0 |
| Active Recalls | 0 |
| Most Recent | 2017-11-01 |
Frequently Asked Questions
When was Aurora Products, INC. last recalled?
The most recent FDA recall involving Aurora Products, INC. was issued on 2017-11-01. Its earliest recorded recall was on 2015-03-20, and it has 6 FDA recalls on record overall.
Does Aurora Products, INC. have any active recalls?
No. None of Aurora Products, INC.'s FDA recalls are currently marked Ongoing — all have been classified as completed or terminated.
How serious have Aurora Products, INC.'s recalls been?
Of Aurora Products, INC.'s 6 FDA recalls, 4 were Class I (a reasonable probability of serious health consequences or death), 2 Class II (possible temporary or reversible health effects), and 0 Class III (unlikely to cause adverse health effects).
Is Aurora Products, INC. safe?
Aurora Products, INC. has had 6 FDA food recalls, including 4 Class I (most serious) recalls. The most recent recall was on 2017-11-01.
More about Aurora Products, INC.
Aurora Products, INC. was last involved in an FDA food recall on 2017-11-01. Its first recorded recall was on 2015-03-20, spanning 6 recalls in total. All of its recalls have since been classified as completed or terminated by the FDA.
This answer pulls from the FDA openFDA enforcement-report API, the authoritative federal source for U.S. FDA food, drug, and device recalls. The headline number above is the direct answer; what follows is the additional context most readers need to use the answer for a real decision rather than just a fact lookup.
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.