PlainRecalls
FDA Devices Moderate Class II Ongoing

LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP);

Reported: October 22, 2025 Initiated: September 11, 2025 #Z-0141-2026

Product Description

LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP);

Reason for Recall

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

Details

Units Affected
0 units
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Location
Marlborough, MA

Frequently Asked Questions

What product was recalled?
LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP);. Recalled by Boston Scientific Corporation. Units affected: 0 units.
Why was this product recalled?
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 22, 2025. Severity: Moderate. Recall number: Z-0141-2026.