Microvention recalls specific Terumo AZUR Peripheral Coil System models due to potential missing implant coils. Affected units may require replacement to prevent complications.
The devices may be missing the implant coil.
Microvention is recalling certain Terumo AZUR Peripheral Coil System models because they might be missing the implant coil. This could lead to improper treatment if used without the coil.
The devices may be missing the implant coil, which is critical for proper treatment. Without the coil, the procedure might not work correctly, potentially leading to ineffective treatment or complications.
Patients who have received the recalled Terumo AZUR Peripheral Coil System models for neurosurgery are most at risk. Healthcare providers using these devices for medical procedures may also be affected.
Check for the product name 'Terumo AZUR Peripheral Coil System, Detachable 18, Framing Coil' with reference numbers 45-681026, 45-681434, 45-682050, or 45-680820. The lot numbers are listed in the description.
Verify the reference number and lot numbers on the device label to confirm if it is affected.
The devices may be missing the implant coil, which is critical for proper treatment.
The recall does not specify a remedy, so check with your healthcare provider for guidance.
The affected models have reference numbers 45-681026, 45-681434, 45-682050, and 45-680820 with specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-1221-2020 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-1221-2020 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.
