Data Foundry

Medical device recalls 2024

ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC… — Class II medical device recall Z-3157-2024

Ongoing recall by MICROVENTION INC., reported 2024-09-25, distributed nationwide. Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years

Recall numberZ-3157-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMICROVENTION INC., Aliso Viejo, CA, United States
Recall initiated2024-08-05
Classified2024-09-17
Reported by FDA2024-09-25
DistributedNationwide (US)
Quantity1,370 devices
Reason classeslabeling
UPC / GTIN / UDI-DI00810170018831, 00810170018848, 00810170018862
Lot numbers0000181279, 0000279433, 0000280707, 0000280790, 0000281275, 0000281276, 0000281277, 0000281278, 0000282116, 0000282616, 0000283271, 0000336496, 0000337041, 0000337055, 0000337865, 0000338960, 0000339787, 0000340323, 0000341352, 000034154, 0000342289, 0000342830, 0000345185, 0000345946, 0000346638, 0000347204, 0000347296, 0000347509, 0000347518, 0000354010, 0000354790, 0000355704, 0000361497, 0000364249, 0000367420, 0000368172, 0000369548, 0000372400, 0000373878, 0000374160 and 67 more
Model numbersER173020, ER173020-US, ER174030, ER174030-US, ER176044, ER176044-US

Product

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.

Reason for recall

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3157-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.