The Recall Desk
ModerateFDA (Drugs)·D-0205-2025·Announced 2025-01-29

Kissable Diabetics Foot Cream recalled nationwide for inadequate release testing

Brands International Corporation is recalling Kissable Diabetics Foot Cream nationwide due to lack of adequate release testing during manufacturing. The FDA has classified this as a Class II recall.

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 II recall for a manufacturing process deviation related to inadequate release testing. No illnesses or injuries have been reported, and the issue is compliance-related rather than a confirmed safety threat. This warrants a Moderate classification per the rubric criteria for voluntary precautionary recalls.

Plain-English summary

Brands International Corporation is recalling Kissable Diabetics Foot Cream, a topical foot cream sold in 4 oz (113 g) tubes and manufactured in Newmarket, Ontario, Canada. The product is distributed nationwide in the United States.

The recall has been issued due to manufacturing deviations involving lack of adequate release testing. The FDA has classified this as a Class II recall.

The affected product includes multiple lot numbers, all within their expiration dates: 23319025, 23318024, 23313023, 23311022, 23310021, 23222021, 23220020, 23215019, 23215018, 23214017, 23213016, 23208015, 2313014, 2312213, 2312212, 2312111, 2312110, 2311709, 2311708, 2311607, 2311506, 2311405, 2307904, 23073003, 23072002, 2306901, and 24135003.

Consumers who have purchased Kissable Diabetics Foot Cream should stop using the product. Those with questions should contact Brands International Corporation regarding returns or replacements.

The recalled product

Product
Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6 72008 80925 3
Manufacturer
Brands International Corporation
Category
Drug — Topical / Foot Care
Hazard
  • cgmp-deviation
  • inadequate-release-testing

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 (20)

  • Lots: 23319025
  • 23318024
  • 23313023
  • 23311022
  • 23310021
  • 23222021
  • 23220020
  • 23215019
  • 23215018
  • 23214017
  • 23213016
  • 23208015
  • 2313014
  • 2312213
  • 2312212
  • 2312111
  • 2312110
  • 2311709
  • 2311708
  • 2311607

Distribution

Distributed nationwide across the United States.

Related recalls

Same category