Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient
Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.
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. The hazard is subpotency (reduced active ingredient and low pH) without any reported illnesses or injuries. The product fails to deliver intended therapeutic effect but does not present an acute safety threat, consistent with a Moderate severity classification.
Plain-English summary
Bell Pharmaceuticals, Inc. is recalling Meijer Earwax Removal Kit containing Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), with washer bulb. The product is being recalled because it is subpotent—the assay shows approximately 0.6% active ingredient instead of the expected 6–7%—and has a low pH value. This means the product will not perform as intended for earwax removal.
The recalled product was distributed nationwide. It is identified by NDC 41250-835-33, Lot 1505344, with an expiration date of April 2027. A total of 993 units were distributed.
Consumers who have purchased this product should discontinue use and consult a healthcare provider if they have questions. For additional information, consumers may contact the FDA at the drug safety and availability portal.
The recalled product
- Product
- MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
- Brand
- MEIJER EARWAX REMOVAL KIT
- Manufacturer
- Bell Pharmaceuticals, Inc
- Category
- Drug — OTC Topical
- Hazard
- Affected units
- 993
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 (2)
- Lot:1505344
- exp 2027-04.
UPCs (1)
- 0708820013537
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 11 recalled by Bell Pharmaceuticals, Inc 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.
See all 11 products in this recall →Related recalls
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