Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated.
Summary
The FDA issued a Class II for Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt. by Albertsons Companies LLC. Reason: Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cros.
Details
Source
Food Recall
External ID
H-0630-2026
Action Date
2026-04-01
Status
Terminated
Category
food
Product Description
Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated. Consumer package is a plastic cup with foil lid and clear plastic lid. UPC 0 21130 07662 8. Distributed by Lucerne Foods, Inc PO Box 99, Pleasanton, CA. Product is distributed in a 6-pack case that consists of a flat cardboard tray and clear plastic film. There are no graphics on the distribution unit. The cases are broken down and product is merchandised as a single 24 oz.
Lot/Code Info: BEST BEFORE MAR 31 2026.
Quantity Affected: 12,222 tubs (24oz. per tub)
Reason for Recall
Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.
Distribution
Distributed in AK, ID, CA, OR, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-16
Company
Boise, ID
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 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Albertsons Companies LLC has 174 FDA actions in our database, including 174 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 (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Albertsons Companies LLC have FDA actions?
Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0630-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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