Medical device recalls Moderate risk

Boston Scientific Corporation recalls CXR Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404461 (12CM PS IZ), (2) 72404462 (14CM PS IZ), (3)…

Recall date
September 11, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0143-2026
FDA classification
Class II
Brand / firm
Boston Scientific Corporation
Sold / distributed
Worldwide distribution - US Nationwide and the country of Canada.

Why it was recalled

The potential for devices to experience inflation and/or deflation performance issues or difficulties.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

CXR Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404461 (12CM PS IZ), (2) 72404462 (14CM PS IZ), (3) 72404463 (16CM PS IZ), (4) 72404464 (18CM PS IZ), (5) 72404465 (10CM IP IZ), (6) 72404466 (12CM IP IZ), (7) 72404467 (14CM IP IZ), (8) 72404468 (16CM IP IZ), (9) 72404469 (18CM IP IZ);

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