Home / Recalls / MICROVENTION INC. / Z-0202-2022

Z-0202-2022 Class II Terminated

Recalled by MICROVENTION INC. — Aliso Viejo, CA

Recall Details

Product Type
Devices
Report Date
November 10, 2021
Initiation Date
October 20, 2021
Termination Date
May 15, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
33

Product Description

Aspiration Syringe Kit, REF: MVSK60

Reason for Recall

Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.

Distribution Pattern

US Nationwide distribution in the states of AL, NY, NV.

Code Information

Lot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461

Other recalls by MICROVENTION INC.

  • Z-0108-2026 Class II — Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED452 (September 5, 2025)
  • Z-2188-2025 Class II — LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 (May 29, 2025)
  • Z-1121-2025 Class II — MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 m (December 11, 2024)
  • Z-0990-2025 Class II — Microvention, Headway" 17 Advanced Straight Microcatheter with Hydrophilic Coati (December 2, 2024)
  • Z-3157-2024 Class II — ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval (August 5, 2024)
  • Z-0868-2024 Class II — TERUMO HydroPearl Compressible Microspheres for Embolisation REF 8HP2S600 (December 21, 2023)
  • Z-0187-2024 Class II — AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324 (August 24, 2023)
  • Z-2238-2023 Class II — FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511 (June 7, 2023)
  • Z-0170-2023 Class II — WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm (September 21, 2022)
  • Z-1829-2021 Class III — VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen ca (April 21, 2021)