Class II · ModerateActive recall
Broadway Joe's Pain Cream
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: T1110, Exp: 1/7/2027; T1111, Exp: 1/9/2027; T1112, Exp: 1/16/2027; T1113, Exp: 1/17/2027; T1114, Exp: 1/17/2027
Where it was soldDistributed in the state of Colorado (US).
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
CGMP Deviations: Potential contamination of raw material
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Lexia LLC |
| NDC | 83088-8120-5 |
Show the full FDA record
| Full product label | Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003 7 |
| Recalling firm | Lexia LLC |
| Distribution | Distributed in the state of Colorado (US). |
| Quantity | 2,400 2 oz-jars |
| Recall initiated | 2026-08-21 |
| Report date | 2026-09-09 |
| Recall completed | — |
| Recall number | D-0828-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Franklin TN United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.