Microvention recalls certain Microplex 10 Platinum Coil Systems for possible missing implant coils, which could lead to incomplete treatment of vascular issues.
The devices may be missing the implant coil.
Microvention is recalling specific models of their Microplex 10 Platinum Coil System for possible missing implant coils. This could result in incomplete treatment of vascular malformations or aneurysms, potentially requiring additional procedures.
The devices may be missing the implant coil, which is critical for properly blocking blood flow to vascular issues. Without the coil, the procedure might not effectively treat the condition, leading to potential need for additional interventions.
Patients undergoing endovascular procedures for vascular malformations or aneurysms who use the recalled Microplex 10 Platinum Coil System are most at risk. Medical professionals using the product for vascular occlusion may also be affected.
Check the product label for the Microplex 10 Platinum Coil System with REF numbers 100203CMSR-V through 100721CMSR-V. The lot numbers listed in the recall include specific combinations like 1903085WP and others.
Look for the REF numbers 100203CMSR-V through 100721CMSR-V on the product label.
The devices may be missing the implant coil, which could lead to incomplete treatment of vascular malformations or aneurysms.
Check the product label for the REF numbers listed in the recall. If you have the recalled product, contact Microvention for further instructions.
The recall states the devices may be missing the implant coil, which could lead to incomplete treatment. However, the hazard does not specify a risk of serious injury in normal use.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1404-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1404-2020 from Microvention. 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.
