Summary
The FDA issued a Class II for Gourmet Burger Roll 12-pack (033474501322) by Piantedosi Baking Co., Inc.. Reason: Products may be contaminated with Cronobacter sakazakii and/or Clostridium botulinum.
Details
Source
Food Recall
External ID
F-1709-2022
Action Date
2022-09-14
Status
Terminated
Category
food
Product Description
Gourmet Burger Roll 12-pack (033474501322)
Lot/Code Info: Lot Codes: 22083; 22088; 22091; 22095; 22101; 22105; 22109; 22112 Expiration: 3/24/2023; 3/29/2023; 4/1/2023; 4/5/2023; 4/11/2023; 4/15/2023; 4/19/2023; 4/22/2023
Quantity Affected: 18,119 frozen product trays (total)
Reason for Recall
Products may be contaminated with Cronobacter sakazakii and/or Clostridium botulinum
Distribution
MA, ME, NH, NY, VT, RI, CT, NJ, VA, FL, NC, SC, IL, MS, CO
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-17
Company
Malden, MA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 129 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Piantedosi Baking Co., Inc. has 18 FDA actions in our database, including 18 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Piantedosi Baking Co., Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Piantedosi Baking Co., Inc. have FDA actions?
Piantedosi Baking Co., Inc. has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1709-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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