Home/Recalls/FDA-Z-2400-2026
FDA DevicesClass II

Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-2...

Published: June 17, 2026Recall ID: Z-2400-2026Category: devicesCountry: US

Reason for Recall / Hazard

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.

Product Description & Identification

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

Affected Products

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

Overview

  • Recalling FirmInter-Med Llc
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of Tennessee and Missouri.
Official Agency Alert