Breads: Ciabatta product 8000 Clear Bag Rolls 8 3.4 oz. Ciabatta product 8652 Clear Bag Rolls 6 5.5 oz.
Summary
The FDA issued a Class II for Breads: Ciabatta product 8000 Clear Bag Rolls 8 3.4 oz. Ciabatta product 8652 C by Klosterman Baking Company. Reason: Products held under insanitary conditions.
Details
Source
Food Recall
External ID
F-0266-2023
Action Date
2023-01-25
Status
Terminated
Category
food
Product Description
Breads: Ciabatta product 8000 Clear Bag Rolls 8 3.4 oz. Ciabatta product 8652 Clear Bag Rolls 6 5.5 oz.
Lot/Code Info: All product delivered between December 12 and December 16. This would include bread items with an expiration date of 12/25/22 and earlier, and any bun items with an expiration date of 12/21/22 and earlier
Quantity Affected: 109,343 (total)
Reason for Recall
Products held under insanitary conditions
Distribution
IN, OH, TN
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-18
Company
Indianapolis, IN
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 84 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Klosterman Baking Company has 26 FDA actions in our database, including 26 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 (Klosterman Baking Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Klosterman Baking Company have FDA actions?
Klosterman Baking Company has 26 FDA actions in our database, including 26 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0266-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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