RecallHawk
Class II Recall

Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, NET WT 14.1oz (400g)

Almondy AB

Summary

The FDA issued a Class II for Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, by Almondy AB. Reason: Metal (stainless steel) object found in retail food product..

Details

Source

Food Recall

External ID

F-0339-2023

Action Date

2023-02-08

Status

Terminated

Category

food

Product Description

Daim, Swedish almond cake with chocolate and crunchy caramel, Baked by Almondy, NET WT 14.1oz (400g)

Lot/Code Info: Lot: L2140 Exp. Date: NOV.18.2023

Quantity Affected: 8325 cakes

Reason for Recall

Metal (stainless steel) object found in retail food product.

Distribution

All 8325 cakes manufactured went to two distribution centers.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-20

Company

Almondy AB

Torslanda, N/A

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

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 (Almondy AB) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Almondy AB have FDA actions?

This is the only FDA action we have on record for Almondy AB in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0339-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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