PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 8, 2023 Initiated: August 24, 2023 #Z-0187-2024

Product Description

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

Reason for Recall

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

Details

Recalling Firm
MICROVENTION INC.
Units Affected
14
Distribution
US Nationwide distribution in the states of TX, NY, VA, NV, MI, CA, AZ, WA.
Location
Aliso Viejo, CA

Frequently Asked Questions

What product was recalled?
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324. Recalled by MICROVENTION INC.. Units affected: 14.
Why was this product recalled?
Peripheral coil system detachable has a potential of unsealed pouch packaging.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 8, 2023. Severity: Moderate. Recall number: Z-0187-2024.