FDA DevicesClass II

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Publicado: 17 de junio de 2026ID de Retiro: Z-2400-2026Categoría: Dispositivos MédicosPaís: Estados Unidos
US
Medical DeviceFDA DevicesUSUS

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Recalling Firm: Inter-Med Llc

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Motivo del Retiro / Peligro

Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.

Descripción del Producto e Identificación

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Productos Afectados

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

Additional Source Details

FieldValue
CityRacine
StateWI
Event id99105
Address 12200 South St
Address 2N/A
Code infoModel No. 504600-28; UDI-DI 00371347008104; Lot Number 2026-0204
Postal code53404-1510
Report date20260617
Product typeDevices
Product quantity500
Reason for recallSome units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260527
Initial firm notificationN/A
Center classification date20260610

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 Devices).

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 Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28?

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 Devices). 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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Resumen

  • Empresa ResponsableInter-Med Llc
  • StatusOngoing
  • Nivel de RiesgoClass II
  • DistributionUS Nationwide distribution in the states of Tennessee and Missouri.
Recall Hazard Severity
High Alert (Class I)
Alerta Oficial de la Agencia

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🚨 SAFETY ALERT: Inter-Med Llc - Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

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https://therecallfile.com/es/recalls/advance-aluminum-chloride-gel-clear-hemostatic-gel-kit-catalog-number/FDA-Z-2400-2026
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