Recall record at a glance
| Official record | F-1862-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bidart Bros. |
| Report date | Apr 8, 2015 |
| Recall initiation date | Dec 22, 2014 |
| Quantity | 33,900 cases; |
| Location | Bakersfield, CA, United States |
Official product description
Gala Apples "Big B"; sold in 40-45 lb. cases with cardboard trays or in 3 lb. poly bags (~12 apples). 5 lb. poly bags (~ 18 apples) and loose fill TriWall containers ~ 700 lbs. Bidart Bros., Bakersfield, CA 93312
Why the product was recalled
Recall of Granny Smith Apples from 2014 harvest used in caramel apple production due to their association with Listeriosis outbreak.. Expanded to include all Granny Smith and Gala apples from 2014 production
Distribution information
CA, MA, NY, MN, PA, MO, WA, TN, TX, MI, AZ, MD, OR, KS, IL, GA, NJ, IA, LA. and Canada. Other foreign distribution has not yet been provided.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.