🔍 RecallPedia

AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324

Class I - Dangerous
🏥 Medical Devices Recalled: August 24, 2023 MICROVENTION Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
MICROVENTION INC.
Reason for Recall:
Peripheral coil system detachable has a potential of unsealed pouch packaging.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324

Product Codes/Lot Numbers:

UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0187-2024

Related Recalls

Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE, FREDX5522-PMA, FREDX3522-PMA, FREDX4525-PMA, FREDX5015-PMA, FREDX5532-PMA, FREDX4013-PMA, FREDX3513-PMA, FREDX4515-PMA, FREDX3517-PMA, MV-F352427X

MICROVENTION

Class I - Dangerous

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 necessitate device recapture and withdrawal of the delivery system and microcatheter together. Insufficient apposition could lead to long-term health consequences.

Sep 5, 2025 Other Medical Devices Nationwide View Details →

LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 +/- 50 micrometers, REF: 8LP2S400

MICROVENTION

Class I - Dangerous

Drug Elutable Microspheres have a smaller actual average diameter that is not within specification, which may lead to inability to reach the desired treatment location (non-targeted embolization), additional procedure/treatment required, blockage other than target vessel, increased procedure time, incomplete embolization, and/or inability to treat the patient.

May 29, 2025 Diagnostic Equipment View Details →

MicoVention Terumo, LVIS Intraluminal Support Device, REF: 213522-CAS, od, 3.5 mm, TL 22 mm, WL 18 mm, Sterile R, CE0297. The intended purpose of the LVIS Device is to serve as a stent-assisted coiling (SAC) device providing support to the embolic coils used in the treatment of wide-necked aneurysms.

MICROVENTION

Class I - Dangerous

Potential for Polytetrafluoethylene (PTFE) material encasing the stent loop may prevent the stent from being pushed out of the introducer.

Dec 11, 2024 Implants & Prosthetics View Details →