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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 7 of 7 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-0138-2026 - TENACIO Pump with InhibiZone; UPN: 72404429; 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0139-2026 - TENACIO Pump without InhibiZone; UPN: 72404420; 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0140-2026 - CX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404486 (15CM IP), (2) 72404488 (21CM IP); 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0144-2026 - LGX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404450 (12CM PS IZ), (2) 72404451 (15CM PS IZ), (3) 72404452 (18CM PS IZ), (4) 72404453 (21CM PS IZ), (5) 72404455 (12CM IP IZ), (6)... 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0142-2026 - CX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404430 (12CM PS IZ), (2) 72404431 (15CM PS IZ), (3) 72404432 (18CM PS IZ), (4) 72404433 (21CM PS IZ), (5) 72404434 (24CM PS IZ), (6) ... 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0143-2026 - 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)... 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
Z-0141-2026 - LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP); 2 10/10/2025 FEI # 3005099803
Boston Scientific Corporation
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