Recall record at a glance
| Official record | F-0293-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Sysco Merchandising and Supply |
| Report date | Jan 25, 2023 |
| Recall initiation date | Dec 14, 2022 |
| Quantity | 962 cases |
| Location | Houston, TX, United States |
Official product description
Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; Greco and Sons Dough Room Product No. 88 Christopher's 14 oz.; Greco and Sons Dough Room Product No. 84 Christopher's 20 oz.; Greco and Sons Dough Room Product No. 86 Christopher's 36 oz.; Greco and Sons Dough Room Product No. 27 Santino 9 oz.; Greco and Sons Dough Room Product No. 10 BULLDOG 8 oz.; Greco and Sons Dough Room Product No. 102 ROMA 12 oz.; Greco and Sons Dough Room Product No.103 ROMA 20 oz.; Greco and Sons Dough Room Product No. 98 TOMATO PIE 12 oz.; Greco and Sons Dough Room Product No. 99 TOMATO PIE 20 oz.
Why the product was recalled
The dough ball products contain the undeclared allergen milk.
Distribution information
OH, PA, VA, WV, IL, MD
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.