meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION
Summary
The FDA issued a Class II for meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41 by Bell Pharmaceuticals, Inc. Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%)..
Details
Source
Drug Recall
External ID
D-0687-2026
Action Date
2026-07-22
Status
Ongoing
Category
drug
Product Description
meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.
Lot/Code Info: Lot:1505344, exp 2027-04.
Quantity Affected: 993 units
Reason for Recall
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Distribution
U.S Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-25
Company
Belle Plaine, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 28 drug recalls issued in the same week, part of 77 drug-related FDA actions this month.
Bell Pharmaceuticals, Inc has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bell Pharmaceuticals, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bell Pharmaceuticals, Inc have FDA actions?
Bell Pharmaceuticals, Inc has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0687-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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