CLASS III ONGOING Drug recall · Reported 31 Jul 2024 · FDA Enforcement Report

Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg recalled

Global Widget is recalling Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, distributed nationwide in the US. The recall was initiated on 25 Jun 2024 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #: 220365, Exp date Oct 2024 ; 230090, Exp. date Feb 2025
Quantity recalled2082 bottles

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-0616-2024
FDA event ID
94838
Recalling firm
Global Widget, Tampa, FL
Classification
Class III
Status
Ongoing
Recall initiated
25 Jun 2024
FDA classified
22 Jul 2024
Reported
31 Jul 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

25 Jun 2024Recall initiated by company
22 Jul 2024Classified by FDA+27 days
31 Jul 2024Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Is Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg recalled?

Yes. Global Widget recalled Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg on 25 Jun 2024. The recall is Class III and its status is Ongoing. Recall number D-0616-2024.

Why was it recalled?

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Which lots are affected?

Lot #: 220365, Exp date Oct 2024 ; 230090, Exp. date Feb 2025

Where was it sold?

Nationwide within the United States

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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