ERIC Retrieval Device
Medical device recall Z-3157-2024. Published in FDA’s Enforcement Report on Sep 25, 2024.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Sep 25, 2024. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word, and 16 states named
- 1,370 devices how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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.
1,370 devices, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Model Number: ER173020-US UDI-DI code: 00810170018831 Lot/Batch Numbers: 0000280707 0000281277 0000282616 0000337055 0000339787 0000341352 0000346638 0000347204 0000347518 0000369548 0000373878 0000383975 0000388574 0000390920 0000408227…
Every code shown here, 1,394 characters
Model Number: ER173020-US UDI-DI code: 00810170018831 Lot/Batch Numbers: 0000280707 0000281277 0000282616 0000337055 0000339787 0000341352 0000346638 0000347204 0000347518 0000369548 0000373878 0000383975 0000388574 0000390920 0000408227 0000413356 0000483914 0000509754 0000552788 0000556936 0000565975 0000584166 0000595486 0000605157 0000610234 0000616881 0000644624 0000648880 0000650593 Model Number: ER174030-US UDI-DI code: 00810170018848 Lot/Batch Numbers: 0000279433 0000281276 0000281278 0000282116 0000283271 0000337041 0000338960 0000342289 0000345185 0000345946 000034154 0000347296 0000364249 0000367420 0000372400 0000375208 0000385910 0000391720 0000394172 0000399765 0000402617 0000406053 0000412461 0000468600 0000472204 0000479549 0000488883 0000548672 0000554916 0000561944 0000563812 0000578999 0000584167 0000588191 0000599947 0000602913 0000619853 0000622476 0000630060 0000655111 Model Number: ER176044-US UDI-DI code: 00810170018862 Lot/Batch Numbers: 0000280790 0000181279 0000281275 0000336496 0000337865 0000340323 0000342830 0000347509 0000354010 0000354790 0000355704 0000361497 0000368172 0000374160 0000387557 0000389821 0000394759 0000401148 0000405396 0000409331 0000466714 0000470240 0000478434 0000481899 0000503647 0000504822 0000556934 0000558955 0000558957 0000563811 0000575805 0000578998 0000582277 0000592294 0000605158 0000619854 0000626526 0000651121
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
U.S. Nationwide distribution in the states of AR, CA, FL, IN, LA, MA, MN, MO, NC, NJ, NY, OH, PA, SC, TX and VA.
The states and territories these words name
16 states and territories.
Every one of them
- Arkansas
- California
- Florida
- Indiana
- Louisiana
- Massachusetts
- Minnesota
- Missouri
- North Carolina
- New Jersey
- New York
- Ohio
- Pennsylvania
- South Carolina
- Texas
- Virginia
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Aug 5, 2024.
- FDA classified it on Sep 17, 2024.
- FDA’s Enforcement Report published it on Sep 25, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- MICROVENTION INC., of Aliso Viejo, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.