Integra LifeSciences recalls SURG STRP 1-1/ 2X6 Model 801454 due to potential endotoxin levels in finished surgical products. Affected items may pose a risk during surgery. Consumers should contact Integra for details.
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 is recalling surgical patties and strips with model number 801454 because they may contain higher-than-expected endotoxin levels. This could potentially cause complications during surgery if used improperly.
The raw material used to make these surgical products may have higher-than-expected endotoxin levels. This could lead to out-of-specification levels in the finished goods, potentially causing complications during surgery.
Surgical professionals and hospitals that use Integra's SURG STRP 1-1/2X6 model 801454 surgical products. The risk is low for endotoxin exposure during normal surgical procedures.
Check for the model number 801454 on the product packaging. Products distributed under JnJ with the same model number are also affected. The recall covers all unexpired items.
Reach out to Integra LifeSciences for specific guidance on affected products and next steps.
The recall indicates potential endotoxin levels in finished goods, but the risk is low for normal surgical procedures. Consult Integra for specific guidance.
The model number is 801454 for SURG STRP 1-1/2X6 surgical patties and strips.
Yes, products distributed under JnJ with the same model number 801454 are included in this recall.
We’ve drafted a message you can send Integra to request your refund or repair — edit it as you like.
Subject: Recall Z-0253-2025 — Integra Integra Hello, I own a Integra that is covered by recall Z-0253-2025 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.
