Foster & Thrive Carbamide Peroxide Recall Issued
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Bell Pharmaceuticals, Inc. is recalling 31,094 units of Foster & Thrive Carbamide Peroxide 6.5% due to subpotent drug levels.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 9, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened Bell Pharmaceuticals, Inc. initiated a voluntary recall of Foster & Thrive Carbamide Peroxide 6.5% because the product is subpotent with low pH and significantly reduced assay (~0.6% vs expected ~6.7%).
Which Products Are Affected Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by McKesson Corp. Affected lots: 1505161, 1505181, 1505301, 1505382, exp 2027-04. A total of 31,094 units were distributed U.S. nationwide.
What You Should Do Consumers should refer to the FDA recall notice for additional guidance.
Why This Matters The Class II recall affects a widely distributed over-the-counter drug product across the United States.
Source FDA recall number D-0686-2026, report date 20260722.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
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Similar body length
Nearest notices by article body length (774 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 9, 2026.
Frequently Asked Questions
Common questions about this FDA recall.