Nature's Script CBD Pain Relief Roll-On Recalled for Subpotent Menthol
FDA Class III recall of Nature's Script CBD Cryotherapy Pain Relief Roll-on (200mg, 1 oz bottles) due to subpotent menthol content less than the labeled 4%. The product did not contain the claimed amount of active ingredient.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class III recall with no reported illnesses or injuries. The hazard is subpotency (menthol content below label claim), which is a potency and labeling issue rather than a safety hazard. Class III recalls are typically scored 1 or 2.
Plain-English summary
Global Widget LLC is recalling Nature's Script CBD Cryotherapy Pain Relief Roll-on in 1 oz bottles containing 200mg of product, distributed nationwide within the United States. The product's menthol potency was less than the 4% stated on the label.
This is an FDA Class III recall. The subpotent menthol means the product does not deliver the claimed amount of active ingredient for pain relief. Affected lot numbers are 230346 (expiration August 2025) and 230090 (expiration February 2025), with a UPC code of 8-40078-56731-5. Approximately 2466 bottles are affected.
Consumers who have purchased this product should check the lot number and expiration date. Those with affected bottles may contact Global Widget LLC at 8419 Sunstate Street, Tampa, Florida 33634, or contact the FDA's Drug Safety and Availability division for further information about the recall.
The recalled product
- Product
- Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
- Manufacturer
- GLOBAL WIDGET LLC
- Category
- Drug — Topical Pain Relief
- Hazard
- Affected units
- 2,466
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot #: 230346
- Exp. date Aug 2025
- 230090 Exp. date Feb 2025
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by GLOBAL WIDGET LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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