Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit Recall
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Inter-Med Llc is recalling 500 units of Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit due to incorrect package inserts that provide wrong first aid instructions.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 28, 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.
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What Happened Inter-Med Llc is recalling certain units of Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit because some units contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically instructing users to induce vomiting in the case of ingestion, while the correct insert instructs users not to induce vomiting.
Which Products Are Affected The recall affects Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28, Model No. 504600-28, UDI-DI 00371347008104, Lot Number 2026-0204. A total of 500 units are affected. Distribution was US Nationwide in the states of Tennessee and Missouri.
What You Should Do Consumers should check their products for the affected lot number and contact the recalling firm for further instructions.
Why This Matters The mislabeled insert could lead users to follow incorrect first aid measures if the product is ingested.
Source FDA recall Z-2400-2026, Inter-Med Llc, Racine, WI.
Original source: FDA Official Notice ↗
Related FDA Recalls
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Similar body length
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Similar severity timing
Same severity (medium) notices issued closest in time to July 28, 2026.
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