FDAFDA recall D-0829-2026 · Sep 9, 2026
Lexia LLC: Broadway Joe's Pain Cream recall
Recall found
Product
Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8 50041 64004 4
Reason for recall
CGMP Deviations: Potential contamination of raw material
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Lot #: 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
- Quantity
- 1,200 4 oz-Jar
- Distribution
- Distributed in the state of Colorado (US).
- Recalling firm
- Lexia LLC, Franklin, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-08-21
Source: openFDA enforcement record D-0829-2026 · search recall number D-0829-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.