Recall record at a glance
| Official record | F-2342-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Arcobasso Foods |
| Report date | Sep 28, 2016 |
| Recall initiation date | Jul 23, 2016 |
| Quantity | 240,000 single bottles |
| Location | Hazelwood, MO, United States |
Official product description
Panera Bread Balsamic Vinaigrette Dressing, NET 20 FL OZ (1.25 PT) 591 mL, most responsible firm on the label is Panera Bread St. Louis, MO 63127 PaneraAtHome.com. Product packaged in plastic bottles and shrink wrapped as a twin pack (2 bottles together). UPC code is 018959753168 for the single bottle. The UPC code for the twin pack is 018959753175.
Why the product was recalled
Consumer complaints of bulging bottles.
Distribution information
Distributed nationwide to Sam's Club only.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Other.
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.