Skip to content
ppharmaranks
Menu
Class IIOngoing

Broadway Joe's Pain Cream recall

FDA recall D-0829-2026 · initiated Aug 21, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Sep 9, 2026How we research

Lexia LLC recalled Broadway Joe's Pain Cream in Aug 2026 — an FDA Class II recall (D-0829-2026) because CGMP Deviations: Potential contamination of raw material.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

CGMP Deviations: Potential contamination of raw material

Something got into the product

A physical or chemical contaminant was found — glass or metal fragments, or a solvent that should not be there.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

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 recalled: 1,200 4 oz-Jar

Details

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
Recalling company
Lexia LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Distributed in the state of Colorado (US).
Initiated
Aug 21, 2026
FDA report date
Sep 9, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Broadway Joe's Pain Cream recalled?
Lexia LLC recalled Broadway Joe's Pain Cream in Aug 2026 — an FDA Class II recall (D-0829-2026) because CGMP Deviations: Potential contamination of raw material. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Broadway Joe's Pain Cream recalled?
Per the FDA enforcement record, the reason for recall D-0829-2026 was: CGMP Deviations: Potential contamination of raw material
Is a recalled Broadway Joe's Pain Cream dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Broadway Joe's Pain Cream are affected?
Distributed: Distributed in the state of Colorado (US).. The recall covers these lots — 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. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0829-2026.

Source: openFDA Drug Enforcement record D-0829-2026 ↗

← All drug recalls