Lexia recall: Broadway Joe's Pain Cream
Lexia LLC is recalling Broadway Joe's Pain Cream because of manufacturing-practice violations – 2,400 2 oz-jars; 1,200 4 oz-Jar. The U.S. Food and Drug Administration published the recall on September 9, 2026; it began on August 21, 2026. Distributed in 1 state (Colorado).
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Broadway Joe's Pain Cream |
| Brand | Lexia |
| Company | Lexia LLC |
| Type | Drugs |
| Classification | Class II |
| Recall date | August 21, 2026 |
| Published by FDA | September 9, 2026 |
| Quantity | 2,400 2 oz-jars; 1,200 4 oz-Jar |
| Recall ID | 99751 |
Recalled products (2)
- 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
- FDA recall number
- D-0828-2026
- 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
- 2,400 2 oz-jars
- Classification
- Class II
- 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
- FDA recall number
- D-0829-2026
- 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
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99751
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Franklin, TN, United States
Why it was recalled
The problem: manufacturing-practice violations.
The reason the FDA lists: “CGMP Deviations: Potential contamination of raw material”
Where it was sold
1 state: Colorado. Distribution as the FDA records it: “Distributed in the state of Colorado (US).”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99751, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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| Oct 7, 2026 | Aurolab Trust recall: FOCUS PI Hypromellose 0.7% FormulaDrugs · 25,220 bottles | a sterility problem Serious | FDA Class II |
| Oct 7, 2026 | Amneal Pharmaceuticals recall: Estradiol GelDrugs · 2,592 30-count cartons | Defective Container; packets were found to be either empty or partially full. Serious | FDA Class II |
About this recall
Is Lexia Broadway Joe's Pain Cream recalled?
Yes. Lexia LLC recalled it on August 21, 2026; FDA published it September 9, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Because of manufacturing-practice violations. The reason given: CGMP Deviations: Potential contamination of raw material
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
In 1 state (Colorado).
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.