Startseite/Alle Rückrufe/FDA-D-0688-2026
FDA DrugsClass II

CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.

Veröffentlicht: 22. Juli 2026Rückruf-ID: D-0688-2026Kategorie: Arzneimittel & MedikamenteLand: Vereinigte Staaten
US
PharmaceuticalFDA DrugsUSUS

CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.

Recalling Firm: Bell Pharmaceuticals, Inc

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Mitteilung übersetzenTranslate notice text, hazard warnings, and descriptions into any supported language.

Grund für den Rückruf / Gefahr

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Produktbeschreibung & Identifikation

CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.

Additional Source Details

FieldValue
CityBelle Plaine
StateMN
Openfda › Upc0041520154446
Openfda › Unii31PZ2VAU81
Openfda › RouteAURICULAR (OTIC)
Openfda › Rxcui702050
Openfda › Spl id0c801757-f335-cd4d-e063-6294a90a433b
Openfda › Brand nameCAREONE EARWAX REMOVAL DROPS
Openfda › Spl set id13a161c6-bc06-4315-9cc9-fe49d046cd6f
Openfda › Package ndc72476-838-34
Openfda › Product ndc72476-838
Openfda › Generic nameCARBAMIDE PEROXIDE
Openfda › Product typeHUMAN OTC DRUG
Openfda › Substance nameCARBAMIDE PEROXIDE
Openfda › Manufacturer nameRetail Business Services, LLC
Openfda › Application numberM014
Openfda › Is original packagertrue
Event id99278
Address 1200 W Beaver St
Code infoLot:1505141, exp 2027-04.
Postal code56011-1894
Report date20260722
Product typeDrugs
Product quantity1,201 units
Reason for recallSubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260625
Initial firm notificationLetter
Center classification date20260714

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, L...?

Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • Rückrufendes UnternehmenBell Pharmaceuticals, Inc
  • StatusOngoing
  • RisikostufeClass II
  • DistributionU.S Nationwide
Recall Hazard Severity
High Alert (Class I)
Offizielle Behördenwarnung

📢 Warnung teilen

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🚨 SAFETY ALERT: Bell Pharmaceuticals, Inc - CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.

Check if your household is affected:
https://therecallfile.com/de/recalls/careone-carbamide-peroxide-6-5-0-5-fl-oz-15-ml-bottle-ndc-72476-838-34/FDA-D-0688-2026
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