RecallHawk
Class II Recall

Pamana Premium Bangus Belly (Cut Deboned Milkfish Belly), 340 g (120 oz)

Foremost Foods International, Inc.

Summary

The FDA issued a Class II for Pamana Premium Bangus Belly (Cut Deboned Milkfish Belly), 340 g (120 oz) by Foremost Foods International, Inc.. Reason: Potential C. botulinum growth and toxin formation. Frozen bangus (milkfish) in reduced oxygen packaging does not contain instructions to keep frozen a.

Details

Source

Food Recall

External ID

F-0693-2024

Action Date

2024-01-10

Status

Terminated

Category

food

Product Description

Pamana Premium Bangus Belly (Cut Deboned Milkfish Belly), 340 g (120 oz)

Lot/Code Info: All product codes

Quantity Affected: 448 boxes

Reason for Recall

Potential C. botulinum growth and toxin formation. Frozen bangus (milkfish) in reduced oxygen packaging does not contain instructions to keep frozen and instructions for proper thawing (e.g., "Important, keep frozen until used, thaw under refrigeration immediately before use.").

Distribution

U.S. Distribution to Supermarkets in CA, HI, WA, IL, NV, and TX. No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-01

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

Foremost Foods International, Inc. has 6 FDA actions in our database, including 6 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 (Foremost Foods International, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Foremost Foods International, Inc. have FDA actions?

Foremost Foods International, Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0693-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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