Recall record at a glance
| Official record | F-2094-2012 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Ciolino Wholesale Produce, Inc. |
| Report date | Sep 5, 2012 |
| Recall initiation date | Aug 17, 2012 |
| Quantity | 7cs-84/8 oz. packages, or a total of 588/8 oz |
| Location | Temperance, MI, United States |
Official product description
Highline Mushrooms Sliced, white mushrooms 8 oz.
Why the product was recalled
On 8/13/12, Highline Mushrooms, of Ontario Canada, voluntarily recalled lots of sliced, white mushrooms that may be contaminated with Listeria monocytogenes. Ciolino Wholesale Produce, Inc. received a shipment of the mushrooms and initiated their own voluntary recall upon receiving notice from Highline Mushrooms.
Distribution information
MI and OH distribution only. Retail only.
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: Press Release.
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.