Recalled Boston Scientific LGX Preconnect with TENACIO Pump with InhibiZone devices may experience inflation and deflation performance issues. Affected units have 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 certain LGX Preconnect devices with TENACIO Pump and InhibiZone for potential inflation and deflation performance issues. This could lead to improper function of the medical device.
The devices may experience inflation and deflation performance issues, which could lead to improper function. This might affect the medical device's ability to work correctly.
Patients using the recalled LGX Preconnect devices with TENACIO Pump and InhibiZone are most at risk. The recall affects specific model sizes and production lots.
Check for UPNs: 72404450 (12CM PS IZ), 72404451 (15CM PS IZ), 72404452 (18CM PS IZ), 72404453 (21CM PS IZ), 72404455 (12CM IP IZ), 72404456 (15CM IP IZ), 72404457 (18CM IP IZ), or 72404458 (21CM IP IZ). Also check the lot numbers listed in the recall notice.
Look for the UPN and lot numbers on your device to confirm if it is affected by this recall.
Boston Scientific is recalling specific LGX Preconnect devices with TENACIO Pump and InhibiZone for potential inflation and deflation performance issues.
Check your device's UPN and lot numbers against the list provided in the recall notice to see if it is affected.
The recall indicates potential inflation and deflation performance issues, which could lead to improper device function, but no specific injuries or deaths have been reported.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0144-2026 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0144-2026 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.
