FDA recall record

Lexia Broadway Joe's Pain Cream, 3000 gm CBD recall — FDA D-0829-2026

CGMP Deviations: Potential contamination of raw material

Class IIclassification
D-0829-2026official record ID
Sep 9, 2026report date

Recall record at a glance

Official recordD-0829-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmLexia LLC
Report dateSep 9, 2026
Recall initiation dateAug 21, 2026
Quantity1,200 4 oz-Jar
LocationFranklin, TN, United States

Official product description

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

Why the product was recalled

CGMP Deviations: Potential contamination of raw material

Distribution information

Distributed in the state of Colorado (US).

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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