Class IITerminated in FDA datasetRecall initiated Dec 18, 2022

Breads: Rye product 1495 Klosterman Retail

Recalling firm: Klosterman Baking Company

Why it was recalled

Products held under insanitary conditions

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 24, 2023.

Check your package

Compare the exact product and package details with the label you have.

ProductBreads: Rye product 1495 Klosterman Retail UPC # 0005172100109 Loaf 1 16 oz. Rye product 1505 Clear Bag Loaf 1 32 oz. Rye product 1525 Klosterman Foodservice UPC # 0005172100456 Loaf 1 24 oz. Rye product 1545 Klosterman Retail UPC # 0005172100108 Loaf 1 16 oz. Rye product 1550 Clear Bag Loaf 1 32 oz. Rye product 1590 Clear Bag Loaf 1 32 oz. Rye product 1595 Clear Bag Loaf 1 32 oz. Rye product 8023 Clear Bag Loaf 1 32 oz. Rye product 8034 Clear Bag Loaf 1 32 oz. Rye product 8221 Clear Bag Loaf 1 32 oz. Rye product 8572 Clear Bag Loaf 1 32 oz.
Package size16 oz

FDA code information

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

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Breads: Rye product 1495 Klosterman Retail UPC # 0005172100109 Loaf 1 16 oz. Rye product 1505 Clear Bag Loaf 1 32 oz. Rye product 1525 Klosterman Foodservice UPC # 0005172100456 Loaf 1 24 oz. Rye product 1545 Klosterman Retail UPC # 0005172100108 Loaf 1 16 oz. Rye product 1550 Clear Bag Loaf 1 32 oz. Rye product 1590 Clear Bag Loaf 1 32 oz. Rye product 1595 Clear Bag Loaf 1 32 oz. Rye product 8023 Clear Bag Loaf 1 32 oz. Rye product 8034 Clear Bag Loaf 1 32 oz. Rye product 8221 Clear Bag Loaf 1 32 oz. Rye product 8572 Clear Bag Loaf 1 32 oz.

Original FDA recall reason

Products held under insanitary conditions

Recall details

Recall number
F-0283-2023
Event ID
91351
FDA status
Terminated
Initiated
Dec 18, 2022
Reported
Jan 25, 2023
Classified
Jan 17, 2023
Terminated
Jan 24, 2023
Quantity
109,343 (total)
Location
Indianapolis, IN, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

IN, OH, TN

FDA source record · F-0283-2023

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.