Penobscot McCrum LLC Recall History
Penobscot McCrum LLC has had 2 FDA-tracked food recalls since 2017. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 2
- Years in FDA Data
- Since 2017
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (2)
- Latest Recall
- Jun 20, 2017
- First Recorded Recall
- Jun 20, 2017
- States Affected
- 26 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Penobscot McCrum LLC recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Jun 20, 2017 | Battered Jo-Jo Wedges / 00047 (5 lb bags) | Class II | Terminated |
| Jun 20, 2017 | Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags) | Class II | Terminated |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Penobscot McCrum LLC has 2 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Penobscot McCrum LLC has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Penobscot McCrum LLC's 2 recalls break down by severity: 0 Class I (may cause serious health issues), 2 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Penobscot McCrum LLC recalls have affected 26 states (nationwide distribution). Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
For this entity, the underlying data on this page comes from the FDA openFDA enforcement-report API. The breakdown above is the federal record; the paragraphs below add the per-entity context that makes the headline numbers usable for a real decision rather than just a data lookup.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.