Severity
Moderate
FDA Drug recall · Reported July 22, 2026
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Bell Pharmaceuticals, Inc recalled TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS I… - a moderate-severity action.
TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS I… was recalled by Bell Pharmaceuticals, Inc in July 22, 2026. Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).. Check the official notice for the remedy. Verify recall #D-0681-2026 with the FDA Drug before acting.
The recall
Bell Pharmaceuticals, Inc issued this moderate-severity FDA Drug recall-SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%)..
Sourced from official FDA Drug enforcement records. Verify recall #D-0681-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0681-2026) was formally reported on July 22, 2026, with the manufacturer initiating the action on June 25, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Bell Pharmaceuticals, Inc is listed as the recalling firm, operating out of Belle Plaine, MN. Federal records list the affected scope as 16,156 units.
The documented reason for this recall is: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). Distribution data in the federal record shows the product reached: U.S Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,436 drugs & medications recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
16,156 units
Related Recalls
6
6 from same agency
TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007.
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0681-2026 |
| Date reported | July 22, 2026 |
| Date initiated | June 25, 2026 |
| Recalling firm | Bell Pharmaceuticals, Inc |
| Firm location | Belle Plaine, MN |
| Affected scope | 16,156 units |
| Distribution | U.S Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Same archive severity grade (Moderate), closest by report date among other firms and states.
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported July 22, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.