MICROVENTION INC. recalls MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R, CE0297. The intended…
Potential for Polytetrafluoethylene (PTFE) material encasing the stent loop may prevent the stent from being pushed out of the introducer.
Read the official notice →- Date
- 2025-02-19
- Country
- United States
- Brand
- Microvention
- Product
- MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R, CE0297. The intended…
- Classification
- Class II
- Units
- US: None OUS: China
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Microvention recalls
- 2026-05-20
USMICROVENTION INC. recalls LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22 mm x 18 mm,…
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress,…
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MICROVENTION INC. recalls Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536,…
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be incompletely open or not properly apposed to the vessel wall, which may…
FDA · DeviceMICROVENTION INC.Worldwide - US Nationwide distribution in the states of SD, CA, SC, TX, FL,…Official notice → - 2025-08-06
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FDA · DeviceMICROVENTION INC.OUS: Italy, Spain, Portugal, Poland, Belgium, Germany, Denmark, France,…Official notice → - 2025-01-29
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FDA · DeviceMICROVENTION INC.U.S. Nationwide distribution in the states of AR, CA, FL, IN, LA, MA, MN, MO,…Official notice → - 2024-02-07
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MICROVENTION INC. recalls TERUMO HydroPearl Compressible Microspheres for Embolisation REF 8HP2S600
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Other drugs & medical recalls in the United States
- 2025-02-19
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Stryker Corporation recalls stryker Precision Thin, Catalog Number REF 2296-003-155; Micro Oscillating and Sagittal Blades
Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.
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