Integra NeuroSciences recalls CODMAN Disposable Perforator 14mm Cranial Perforators with inadequate welds that could cause disassembly. Affected units have specific model numbers and lot numbers listed in the recall. Consumers should check their product details and contact Integra for remedies.
Inadequate weld that can potentially cause the product to disassemble.
Integra NeuroSciences is recalling CODMAN Disposable Perforator 14mm Cranial Perforators due to a potential weld issue that could cause the product to disassemble. This is a low-risk issue that doesn't involve serious injury but requires checking your product details to ensure you have the affected models.
The product has an inadequate weld that could cause it to disassemble during use. This might lead to the instrument becoming unstable or malfunctioning, but it does not pose a risk of serious injury or death.
Medical professionals who use these surgical instruments are most likely affected. The recall targets specific model numbers and lot numbers listed in the product details.
Check your CODMAN Disposable Perforator 14mm Cranial Perforator for model number 261221 and lot numbers listed in the recall (e.g., 5580821, 5664307, etc.).
Identify your CODMAN Disposable Perforator 14mm Cranial Perforator model number (261221) and lot numbers from the list provided in the recall.
The affected model number is 261221.
Check your product's model number (261221) and lot number against the list of affected lot numbers provided in the recall.
Contact Integra NeuroSciences for further instructions on how to handle the affected product.
We’ve drafted a message you can send Integra NeuroSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1716-2025 — Integra NeuroSciences Integra NeuroSciences Hello, I own a Integra NeuroSciences that is covered by recall Z-1716-2025 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.
