Integra LifeSciences recalls Cytal Burn Matrix 7x10 cm patches with potential increased endotoxin levels. Affected lots include 7579683, 7579681, 7582227, 7583891, 7594266, 7593018, 7593011, 7593013. No action needed per recall.
Increased rate of out-of-specification endotoxin results.
Integra LifeSciences is recalling Cytal Burn Matrix 7x10 cm patches due to potential increased endotoxin levels. This could pose a risk of infection or adverse reactions if used medically. The recall does not require immediate action for users.
Endotoxins are natural components of bacterial cell walls that can cause infections or adverse reactions when introduced into the body. The recall indicates these patches may have higher-than-expected endotoxin levels, potentially increasing infection risk during medical use.
Users of Cytal Burn Matrix 7x10 cm patches with lot numbers 7579683, 7579681, 7582227, 7583891, 7594266, 7593018, 7593011, or 7593013 are most at risk. Medical users should check their patch lot numbers.
Check the lot number on your Cytal Burn Matrix 7x10 cm patch. Affected lots are 7579683, 7579681, 7582227, 7583891, 7594266, 7593018, 7593011, and 7593013. The product ID is BMM0710.
Look for the lot number on your Cytal Burn Matrix 7x10 cm patch to see if it matches the affected lots listed.
No action is required per the recall. The product is safe to use if the lot number is not affected.
The recall indicates a potential increase in endotoxin levels, which could lead to infection or adverse reactions. However, the recall does not specify serious injury risks.
Check the lot number on your patch against the affected lots: 7579683, 7579681, 7582227, 7583891, 7594266, 7593018, 7593011, and 7593013.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1819-2026 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-1819-2026 from Integra LifeSciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
