Breads Wheat product 1305 Klosterman Foodservice recall

Recalled by Klosterman Baking Company · Indianapolis, IN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Products held under insanitary conditions

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Breads: Wheat product 1305 Klosterman Foodservice UPC # 0005172100452 Loaf 1 28 oz. Wheat product 1306 Clear Bag Loaf 1 32 oz. Wheat product 1310 Clear Bag Loaf 1 24 oz. Wheat product 1358 Klosterman Retail UPC # 0005172100714 Loaf 1 24 oz. Wheat product 1380 Pennington Retail (Klosterman) UPC # 0005172100221 Loaf 1 20 oz. Wheat product 1400 Klosterman Retail UPC # 0005172100371 Loaf 1 12 oz. Wheat product 1920 Clear Bag Loaf 1 24 oz. Wheat product 1962 Clear Bag Loaf 1 28 oz.

Quantity: 109,343 (total)

Food: Bread & bakery

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Indiana Ohio Tennessee

FDA's distribution note: IN, OH, TN

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Klosterman Baking Company
Initiated by: Voluntary: Firm initiated
Recall initiated: Dec 18, 2022
In FDA report of: Jan 25, 2023
Terminated: Jan 24, 2023
FDA recall number: F-0286-2023 · event 91351
Official record: FDA enforcement report search

Also recalled with it (25 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Processing Dec 18, 2022