MICROVENTION INC.: Medical Device Recall in 2023 - (Recall #: Z-0187-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 24, 2023

Date Posted: November 8, 2023

Recall Number: Z-0187-2024

Event ID: 93147

Reason for Recall:

Peripheral coil system detachable has a potential of unsealed pouch packaging.

Status: Ongoing

Product Quantity: 14

Code Information:

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

Distribution Pattern:

US Nationwide distribution in the states of TX, NY, VA, NV, MI, CA, AZ, WA.

Voluntary or Mandated:

Voluntary: Firm initiated