Reported Nov 8, 2023 · Ongoing

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

Microvention Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MICROVENTION INC. · 35 Enterprise · Aliso Viejo, CA · 92656

Is this the product you have?

  • AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM
  • REF45-751324
Lot codes and dates
  • UDI-DI00812636021089
  • Lot0000190693
  • Expiration4/30/2027
Amount recalled
14

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:53 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.