RecallHawk
Class I Recall

Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carn

Optimal Carnivore, LLC

Summary

The FDA issued a Class I for Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. St by Optimal Carnivore, LLC. Reason: Potential for contamination with salmonella..

Details

Source

Food Recall

External ID

F-0756-2025

Action Date

2025-05-14

Status

Terminated

Category

food

Product Description

Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carnivore LLC 1603 Capitol Ave Ste 310 WY371 Cheyenne, WY 82001

Lot/Code Info: Expiration date 12/2026. Lot # 1224064

Quantity Affected: 1483 bottles

Reason for Recall

Potential for contamination with salmonella.

Distribution

Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-15

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 22 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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

How often does Optimal Carnivore, LLC have FDA actions?

This is the only FDA action we have on record for Optimal Carnivore, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0756-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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