RecallHawk
Class II Recall

Multiple FDA-regulated products. Pallets

Inmar Supply Chain Solutions, LLC

Summary

The FDA issued a Class II for Multiple FDA-regulated products. Pallets by Inmar Supply Chain Solutions, LLC. Reason: Potential exposure to rodents and rodent activity in the warehouse..

Details

Source

Food Recall

External ID

F-1449-2023

Action Date

2023-08-30

Status

Terminated

Category

food

Product Description

Multiple FDA-regulated products. Pallets

Lot/Code Info: All food, dietary supplements, and/or cosmetics products that are still within the expiration date purchased from Inmar Supply Chain Solutions, LLC. located in Texas from May 2022 to present.

Quantity Affected: Unknown

Reason for Recall

Potential exposure to rodents and rodent activity in the warehouse.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-08-15

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

Inmar Supply Chain Solutions, 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 (Inmar Supply Chain Solutions, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Inmar Supply Chain Solutions, LLC have FDA actions?

Inmar Supply Chain Solutions, 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-1449-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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