Microvention recalls ERIC Retrieval Devices with incorrect 5-year expiration dates (should be 3 years). Affected models include ER173020, ER174030, and ER176044. Contact for details.
Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years) which extends beyond their true expiration date.
Microvention is recalling ERIC Retrieval Devices that have incorrect expiration dates listed as 5 years instead of the required 3 years. This could lead to device failure after the true expiration date, potentially causing safety issues during medical procedures.
The device's expiration date is incorrectly labeled as 5 years instead of the standard 3 years. This means the device could become ineffective or unsafe after the true expiration date, potentially causing complications during medical procedures.
Healthcare professionals using the ERIC Retrieval Device for stroke treatment are most at risk. Patients receiving the device during procedures may be affected if the device expires prematurely.
Check for model numbers ER173020, ER174030, or ER176044 on the device. The lot/batch numbers listed in the recall notice also identify affected units.
Verify the expiration date on the device label; it should be 3 years from the manufacturing date, not 5 years.
The device has incorrect expiration dates labeled as 5 years instead of the required 3 years, which could lead to device failure after the true expiration date.
Check for model numbers ER173020, ER174030, or ER176044 on the device. Affected units also have specific lot/batch numbers listed in the recall notice.
Contact Microvention directly to confirm if your device is affected and follow their instructions for verification or replacement.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-3157-2024 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-3157-2024 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.
