Integra LifeSciences recalls Codman Cranial Access Kits with incorrect expiration dates on outer boxes. Using past expiration may cause pain, infection, or tissue reactions. Affected kits have specific product numbers and lot numbers.
Incorrect extended expiration dates identified on the outer box label only, if product is used past the correct expiration date there is a potential for pain, infection, or adverse tissue reaction to occur
Integra LifeSc: Recalls Codman Cranial Access Kits that have incorrect expiration dates on the outer box. Using these kits past the correct expiration date could lead to pain, infection, or adverse tissue reactions.
The outer box labels have incorrect expiration dates. If the kit is used after the correct expiration date, it may cause pain, infection, or adverse tissue reactions.
Healthcare professionals using Codman Cranial Access Kits for intracranial pressure monitoring or cerebrospinal fluid drainage procedures. Those with the specific product numbers and lot numbers are most at risk.
Check the outer box label for expiration dates. Affected kits have product number 826614 and lot numbers 20LDC222 or 21HDC461.
Look for the expiration date on the outer box label. If it's incorrect, stop using the kit.
The outer box labels have incorrect expiration dates, which could lead to pain, infection, or adverse tissue reactions if used past the correct expiration date.
Product number 826614 with lot numbers 20LDC222 or 21HDC461.
The recall record does not mention a return or disposal requirement.
We’ve drafted a message you can send Integra LifeSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0817-2022 — Integra LifeSciences Integra LifeSciences Hello, I own a Integra LifeSciences that is covered by recall Z-0817-2022 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.
