Micro Therapeutics recalls MindFrame Capture LP Revascularization Devices (product numbers REF 300010-300018) due to potential partial detachment from delivery wire, which could cause stroke complications.
There is a potential issue for all MindFrame Capture devices to partially detach or separate from the delivery wire.
Micro Therapeutics recalls MindFrame Capture LP devices that may partially detach from the delivery wire during stroke treatment. This could lead to incomplete blood flow restoration and complications if the device separates during use.
The devices may partially detach from the delivery wire during use, which could cause incomplete blood flow restoration. This might lead to complications if the device separates while treating a stroke.
Patients receiving stroke treatment with the MindFrame Capture LP devices are most at risk. Medical professionals using these devices for thrombus removal in intracranial vessels are affected.
Check for product numbers REF 300010 through REF 300018 on the device packaging. The devices are intended for use in stroke treatment within 8 hours of symptom onset.
Look for product numbers REF 300010 through REF 300018 on the device packaging to confirm if it is recalled.
The recall is due to a potential issue where MindFrame Capture LP devices may partially detach from the delivery wire during use, which could cause incomplete blood flow restoration.
Check the product number on the packaging. If it is REF 300010 through REF 300018, contact Micro Therapeutics for further instructions.
The recall states there is a potential for partial detachment, which could lead to complications during stroke treatment, but the record does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Micro Therapeutics to request your refund or repair — edit it as you like.
Subject: Recall Z-1701-2018 — Micro Therapeutics Micro Therapeutics Hello, I own a Micro Therapeutics that is covered by recall Z-1701-2018 from Micro Therapeutics. 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.
