CLASS II ONGOING Drug recall · Reported 9 Sep 2026 · FDA Enforcement Report
Broadway Joe's Pain Cream, (Histamine Dihydrochloride recalled by Lexia
Lexia is recalling Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg, distributed in Colorado. The recall was initiated on 21 Aug 2026 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0828-2026
- FDA event ID
- 99751
- Recalling firm
- Lexia, Franklin, TN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 21 Aug 2026
- FDA classified
- 2 Sep 2026
- Reported
- 9 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Creams, Ointments & Gels
Timeline
| 21 Aug 2026 | Recall initiated by company | |
| 2 Sep 2026 | Classified by FDA | +12 days |
| 9 Sep 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: Potential contamination of raw material
Product as listed by the FDA
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
Where it was distributed
Distributed in the state of Colorado (US).
Questions about this recall
Why was it recalled?
CGMP Deviations: Potential contamination of raw material
Which lots are affected?
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
Where was it sold?
Distributed in the state of Colorado (US).
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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.
Other products in this recall event
1 other product · FDA event 99751| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Broadway Joe's Pain Cream, 3000 gm CBD recalled by Lexia | Lexia | Manufacturing (CGMP) Deviations | CO |
More recalls from Lexia
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Broadway Joe's Pain Cream, 3000 gm CBD recalled by Lexia | Lexia | Manufacturing (CGMP) Deviations | CO |
Other Broadway Joe's Pain recalls
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Broadway Joe's Pain Cream, 3000 gm CBD recalled by Lexia | Lexia | Manufacturing (CGMP) Deviations | CO |