Integra LifeSciences recalls SURG STRP 1/4X6 Model 80145: Higher endotoxin levels in surgical products may pose health risks during surgery. Affected products have UDI numbers 10381780515067 and 20886704036583.
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in finished goods
Integra LifeSciences recalls surgical patties and strips with model number 801450 due to higher-than-expected endotoxin levels in the raw materials. This could potentially lead to health issues during surgery, especially for patients undergoing procedures involving the central nervous system.
The raw materials used to make these surgical products contain higher-than-expected levels of endotoxin. Endotoxins are natural components of bacteria that can cause inflammation or infection if they enter the body during surgery, particularly in sensitive areas like the central nervous system.
Patients and medical professionals who use Integra's surgical patties and strips for central nervous system procedures. Those with the specific model number 801450 are most at risk.
Check for the model number 801450 on the product packaging. Products distributed under JnJ with the same model number also have UDI numbers 10381780515067 and 20886704036583.
Look for the model number 801450 on the packaging or product label.
Integra LifeSciences identified higher-than-expected levels of endotoxin in the raw materials used to produce these surgical products, which could lead to health risks during surgery.
The model number is 801450.
Yes, the UDI numbers are 10381780515067 and 20886704036583.
We’ve drafted a message you can send Integra to request your refund or repair — edit it as you like.
Subject: Recall Z-0249-2025 — Integra Integra Hello, I own a Integra that is covered by recall Z-0249-2025 from Integra. 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.
