MICROVENTION INC. AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
Brand
MICROVENTION INC.
Lot Codes / Batch Numbers
UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027
Products Sold
UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027
MICROVENTION INC. is recalling AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324 due to Peripheral coil system detachable has a potential of unsealed pouch packaging.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Peripheral coil system detachable has a potential of unsealed pouch packaging.
Recommended Action
Per FDA guidance
On 8/22/23, recall notices were mailed to customers, who were asked to do the following: 1) Stop using, quarantine, and return affected devices to the firm. 2) Complete and return the customer acknowledgement form via email to recalls@microvention.com. Inquires can be directed to customer service at 800-990-8368
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026