Microvention recalls AZUR CX 35 Peripheral Coil System Detachable due to potential unsealed pouch packaging. Learn if you have the affected model and what to do.
Peripheral coil system detachable has a potential of unsealed pouch packaging.
Microvention is recalling its AZUR CX 35 Peripheral Coil System Detachable because the packaging might be unsealed. This could lead to contamination or improper use of the medical device. Affected users should check their product details and follow the official recall instructions.
The peripheral coil system detachable may have unsealed pouch packaging, which could lead to contamination or improper use of the medical device. This poses a low risk of infection or incorrect application during medical procedures.
Patients using the AZUR CX 35 Peripheral Coil System Detachable for medical procedures are likely affected. Those with the specific model number and lot code from the recall list are at higher risk.
Check for the model name 'AZUR CX 35 Peripheral Coil System Detachable' and the lot code '0000190693' on the packaging. The product was sold with a specific expiration date of April 30, 2027.
Look for the model name 'AZUR CX 35 Peripheral Coil System Detachable' and lot code '0000190693' on the packaging.
The recall indicates a potential unsealed pouch packaging, which could lead to contamination or improper use. However, the hazard is described as low risk.
Check for the model name 'AZUR CX 35 Peripheral Coil System Detachable' and lot code '0000190693' on the packaging.
The recall does not specify a remedy, so contact Microvention directly for further instructions.
We’ve drafted a message you can send Microvention to request your refund or repair — edit it as you like.
Subject: Recall Z-0187-2024 — Microvention Microvention Hello, I own a Microvention that is covered by recall Z-0187-2024 from Microvention. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
