Boston Scientific recalls TENACIO Pumps without InhibiZone due to potential inflation and deflation performance issues. Affected units have specific lot numbers and were sold in the U.S. Learn what to do.
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific is recalling TENACIO Pumps without InhibiZone because they may have inflation or deflation problems. This could lead to improper function of the device, but the recall does not mention immediate injury risks.
The pumps may experience inflation or deflation issues, which could cause improper function. This might lead to the device not working correctly but does not indicate immediate injury risks.
Patients using TENACIO Pumps without InhibiZone are likely affected. Those with specific lot numbers (1100720566, 1100720567, 1100720568) are most at risk.
Check for lot numbers 1100720566, 1100720567, or 1100720568 on the TENACIO Pump without InhibiZone. These units were sold in the U.S. and are identified by the unique product number UPN: 72404420.
Look for lot numbers 1100720566, 1100720567, or 1100720568 on the pump.
The pumps may experience inflation or deflation performance issues, which could lead to improper function.
Check for lot numbers 1100720566, 1100720567, or 1100720568 on the TENACIO Pump without InhibiZone.
The recall does not specify a need to stop using the pump immediately; it focuses on checking lot numbers.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0139-2026 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0139-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
