Microvention recalls HydroFrame 18 and HydroCoil Embolic Systems due to potential missing implant coils. Affected units have specific REF numbers and lot codes. Consumers should check their product details.
The devices may be missing the implant coil.
Microvention is recalling its HydroFrame 18 and HydroCoil Embolic Systems because some units may be missing the implant coil. This could lead to improper treatment of vascular issues if used without the coil. Affected products have specific reference numbers and lot codes.
The devices may be missing the implant coil, which is critical for properly blocking blood flow to vascular issues. Without the coil, the procedure could fail to treat the condition effectively.
Patients undergoing endovascular procedures for vascular malformations or aneurysms may own these devices. Medical professionals using the systems for embolization are most at risk.
Check the product label for reference numbers like 180723HFRM-V, 180931HFRM-V, or MV-80619HHFA. The lot codes include numbers such as 1904175P7 or 1905025W7.
Look for reference numbers on the label, such as 180723HFRM-V or MV-80619HHFA, and associated lot codes.
The devices may be missing the implant coil, which is critical for properly blocking blood flow during endovascular procedures.
Affected units include reference numbers 180723HFRM-V, 180931HFRM-V, 181644HFRM-V, MV-80619HHFA, MV-80827HHFA, MV-80931HHFA, and MV-81036HHFA.
Check the product label for reference numbers like 180723HFRM-V or MV-80619HHFA and associated lot codes such as 1904175P7.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1403-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1403-2020 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.
