RecallHawk
Class II Recall

L&B Beautiful Morning Glory Muffins. Product #49025. 4 muffins per container. Net Wt 14 oz. UPC 18169-49025.

Lunds Mitchell Rd LLC

Summary

The FDA issued a Class II for L&B Beautiful Morning Glory Muffins. Product #49025. 4 muffins per container. by Lunds Mitchell Rd LLC. Reason: Foreign material (metal).

Details

Source

Food Recall

External ID

F-1744-2024

Action Date

2024-08-28

Status

Terminated

Category

food

Product Description

L&B Beautiful Morning Glory Muffins. Product #49025. 4 muffins per container. Net Wt 14 oz. UPC 18169-49025.

Lot/Code Info: Lot: 301355

Quantity Affected: 1092 units

Reason for Recall

Foreign material (metal)

Distribution

MN

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-25

Company

Lunds Mitchell Rd LLC

Eden Prairie, MN

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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lunds Mitchell Rd LLC has 3 FDA actions in our database, including 3 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 (Lunds Mitchell Rd LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lunds Mitchell Rd LLC have FDA actions?

Lunds Mitchell Rd LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1744-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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