Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; Greco and Sons Dough Room Product No. 88 Christopher's 14 oz.
Summary
The FDA issued a Class I for Greco and Sons Dough Room Product No. 333 PUB DOUGH 9 oz.; Greco and Sons Dough by Sysco Merchandising and Supply. Reason: The dough ball products contain the undeclared allergen milk..
Details
Source
Food Recall
External ID
F-0293-2023
Action Date
2023-01-25
Status
Terminated
Category
food
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.
Lot/Code Info: Best if Used By Date between 12/1/2022 and 06/01/2023
Quantity Affected: 962 cases
Reason for Recall
The dough ball products contain the undeclared allergen milk.
Distribution
OH, PA, VA, WV, IL, MD
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-14
Company
Houston, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 84 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Sysco Merchandising and Supply has 12 FDA actions in our database, including 12 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Sysco Merchandising and Supply) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Sysco Merchandising and Supply have FDA actions?
Sysco Merchandising and Supply has 12 FDA actions in our database, including 12 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0293-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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