ERIC Retrieval Device ER174030-USRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810170018848), received between May 3, 2024 and May 3, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Aug 5, 2024Open, Classified

   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.

   Z-3157-2024 · Root cause: Under Investigation by firm · FDA record ↗

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 3, 2024Material Separation; Stretched; Material Separation; Stretched

  IT WAS REPORTED THAT THE CLOT RETRIEVER DEVICE WAS USED DURING A STROKE CASE. REPORTEDLY, AFTER USE AND REMOVAL FROM THE PATIENT AND ON THE BACK TABLE, IT WAS NOTED THAT THE DISTAL 5MM TIP OF THE LEAD WIRE STRETCHED AND CAME APART AT SOME POINT AFTER SECOND PASS. THE CASE WAS SUCCESSFULLY COMPLETED WITH ANOTHER DEVICE OF THE SAME MODEL. THE PATIENT IS FINE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19238204 ↗