Boston Scientific recalls CXR Preconnect with TENACIO Pump with InhibiZone devices that may experience inflation or deflation performance issues. Affected units include specific UPNs and lot numbers listed in the recall notice.
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific is recalling CXR Preconnect devices with TENACIO Pump and InhibiZone that may have inflation or deflation performance issues. This could lead to improper function of the device, but the recall does not specify a risk of injury or serious harm.
The devices may experience inflation and/or deflation performance issues, which could lead to improper function. However, the recall does not mention any risk of injury or serious harm to users.
Patients using the CXR Preconnect with TENACIO Pump and InhibiZone devices with the specific UPNs and lot numbers listed in the recall notice. Medical professionals who have these devices in their practice are most at risk.
Check if your device has a UPN code (72404461-72404469) and the corresponding lot numbers listed in the recall notice. The devices are used in medical procedures and are typically sold to healthcare providers.
Identify your device's UPN code and lot numbers to confirm if it is affected by this recall.
The recall states potential for inflation and deflation performance issues, but does not mention any risk of injury or serious harm.
Check if your device has a UPN code (72404461-72404469) and the corresponding lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Boston Scientific directly for further instructions.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0143-2026 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0143-2026 from Boston Scientific. 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.
