ERIC Retrieval Device ER173020-USRecalls & reported problems
Microvention, Inc. · ERIC 3 · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810170018831), received between Dec 30, 2024 and Dec 30, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Recalls naming this device
- 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
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
- Stroke/CVA1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 30, 2024Break; Break
ADDITIONAL INFORMATION WAS PROVIDED THAT STATED THE PATIENT'S ANATOMY WAS TORTUOUS WHICH MADE IT DIFFICULT TO REMOVE THE DEVICE, AND IT BROKE. THE PATIENT'S CONDITION REMAINS THE SAME AS STROKE SCALE OF NIHSS 20. NO FURTHER INFORMATION IS AVAILABLE FOR THIS CASE.
Patient problems: Foreign Body In Patient; Stroke/CVA
MAUDE report 21039650 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.