CLASS I Food recall · Reported 14 May 2025 · FDA Enforcement Report
Bone & Joint Restore recalled by Optimal Carnivore
Optimal Carnivore is recalling Bone & Joint Restore, distributed nationwide in the US. The recall was initiated on 15 Apr 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0756-2025
- FDA event ID
- 96713
- Recalling firm
- Optimal Carnivore, Cheyenne, WY
- Brand
- Bone
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 15 Apr 2025
- FDA classified
- 5 May 2025
- Reported
- 14 May 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Dietary Supplements
Timeline
| 15 Apr 2025 | Recall initiated by company | |
| 5 May 2025 | Classified by FDA | +20 days |
| 14 May 2025 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential for contamination with salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
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
Where it was distributed
Nationwide.
Questions about this recall
Why was it recalled?
Potential for contamination with salmonella.
Which lots are affected?
Expiration date 12/2026. Lot # 1224064
Where was it sold?
Nationwide.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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