Integra NeuroSciences recalls CODMAN Disposable Perforators 11mm and 9mm models with inadequate welds. Affected units have specific lot numbers and expiration dates. Consumers should check their product details.
Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.
Integra NeuroSciences is recalling CODMAN Disposable Perforators 11mm and 9mm models due to inadequate welds that could lead to improper use. This recall expands the previous recall for size 14mm units.
The perforators have inadequate welds, which may cause improper function during surgical procedures. This could lead to ineffective use or potential complications if the tool does not perform as intended.
Medical professionals using these surgical tools are most likely affected. Patients and caregivers should check if they own the recalled models.
Check for model numbers 261222, lot numbers listed in the description, and expiration dates between April 2028 and July 2029. The product is a cranial perforator used in surgery.
Look for model number 261222 and lot numbers in the list provided in the recall notice.
The recall is for inadequate welds in the perforators that could lead to improper function during surgical procedures.
Affected models are CODMAN Disposable Perforators 11mm and 9mm with specific lot numbers and expiration dates between April 2028 and July 2029.
No action is required beyond checking if your product matches the affected details. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Integra NeuroSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0373-2026 — Integra NeuroSciences Integra NeuroSciences Hello, I own a Integra NeuroSciences that is covered by recall Z-0373-2026 from Integra NeuroSciences. 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.
