Fresh Recalls

FDAClass II · Drug · Recall D-0828-2026 · Recalled September 9, 2026

Broadway Joe's Pain Cream recall — Lexia LLC

Agency report date: September 9, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Broadway Joe's Pain Cream
Company / brand
Lexia
Lot / serial / date codes
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
Distribution
Distributed in the state of Colorado (US).
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: CGMP Deviations: Potential contamination of raw material

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Broadway Joe's Pain Cream recall status

3. Open the official notice or contact

Official recall ID
D-0828-2026
Brand
All Lexia recalls
Classification
Class II
Units affected
2,400 2 oz-jars
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Franklin, TN, United States
Firm address
367 Riverside Dr Ste 100, N/A, 37064-8977

Identifying details (verbatim from the notice)

Product codes / 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
Distribution
Distributed in the state of Colorado (US).
Firm notified the public via
Letter
FDA event ID
99751
Recall initiated
August 21, 2026
FDA classified
September 2, 2026
FDA report date
September 9, 2026

Other drug recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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