Integra LifeSciences recalls Cytal Wound Matrix 2-Layer 7x10 cm (WSM0710) due to increased endotoxin levels. Affected lots include 7579683 to 7594288. Contact for return instructions.
Increased rate of out-of-specification endotoxin results.
Integra LifeSciences is recalling Cytal Wound Matrix 2-Layer 7x10 cm products with specific lot numbers because they may have higher endotoxin levels. This could pose a risk for people using the product in medical settings, though the exact health impact isn't specified in the recall.
The product may contain higher levels of endotoxins, which are bacterial components that can cause adverse reactions in sensitive individuals. However, the recall does not specify serious injury risks or death.
Medical professionals and patients using the Cytal Wound Matrix 2-Layer 7x10 cm for wound care. Those with the listed lot numbers are most at risk.
Check the product label for the lot numbers listed: 7579683, 7582225, 7583893, 7582227, 7583933, 7583891, 7591942, 7591944, 7583935, 7594266, 7594288, 7594286, 7593011, 7594284, 7593013.
Look for the lot number on the product label to determine if it is affected.
Reach out to Integra LifeSciences for instructions on returning the product.
The product may have increased endotoxin levels, which are bacterial components that could cause adverse reactions in sensitive individuals.
Check the product label for the lot numbers listed: 7579683, 7582225, 7583893, 7582227, 7583933, 7583891, 7591942, 7591944, 7583935, 7594266, 7594288, 7594286, 7593011, 7594284, 7593013.
The recall does not specify a need to stop using immediately; contact Integra LifeSciences for instructions.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1817-2026 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-1817-2026 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.
