Reported Mar 4, 2020 · Terminated
MicroVention Terumo Microplex 18, Platinum Embolization Coil, Cosmos 18, Sterile, Rx, REF numbers 180619CS-V,…
Microvention, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Microvention, Inc. · 35 Enterprise · Aliso Viejo, CA · 92656-2601
Is this the product you have?
MicroVention Terumo Microplex 18Platinum Embolization CoilCosmos 18SterileRxREF numbers 180619CS-V180723CS-V180827CS-V180931CS-V181036CS-V181139CS-V181243CS-V181347CS-V181451CS-V181652CS-V181859CS-V182065CS-V182263CS-Vand 182468CS-V
- Product UsageThe MCS is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature. The firm name on the label is MicroVention, Inc., Tustin, CA
- Lot codes and dates
- Catalog/lot numbers
98 of 98 codes
180619CS-V - 1903065W11904015P11904225W11904295W11905085P11905085W11905175W1and 1905205W1180723CS-V - 1903085W11903185W11904015P11904175P11904295W11905085W1and 1905175W1180827CS-V - 1903205W11904015P11905155W1and 1905205W1180931CS-V - 1904225R11903205W11905175W1and 1905225W1181036CS-V - 1904035R11903085W11903185W11904225W11904265W11905035W11905065W11905175W1and 1905205W1181139CS-V - 1903015L11903015W11903085P11903085W11903185W11904015P11904245P1and 1904245W1181243CS-V - 1903015L11903015W11903065W11903185W11904015P11904175P11904225W11904265W11904295W11905155W11905175W1and 1905225W1181347CS-V - 1903085V11903135R11904035R11903015W11903085W11903205P11903205W1and 1904225W1
- Catalog/lot numbers
- Amount recalled
- 403 units
This recall covers 16 products
The agency filed one notice per product. You are reading one of them; the other 15 are below.
3 more are in the archive.
Where it was sold
Why it was recalled
The devices may be missing the implant coil.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Microvention, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.