Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Recalled by MICROVENTION INC. Due to Due to Retrieval Device product labels stating the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MICROVENTION INC. directly.
Affected Products
ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood flow by effectively removing clots from occlusive vasculature in patients suffering from acute ischemic stroke.
Quantity: 1,370 devices
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MICROVENTION INC.
MICROVENTION INC. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report