medical MODERATE Updated 2023-11-08

MICROVENTION INC. recalls AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, R

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Recalled Product

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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00812636021089, Lot: 0000190693, Expiration: 4/30/2027

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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View official government recall

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