Data Foundry

Medical device recalls 2025

LGX Preconnect with TENACIO Pump with InhibiZone — Class II medical device recall Z-0144-2026

Ongoing recall by Boston Scientific Corporation, reported 2025-10-22, distributed nationwide. The potential for devices to experience inflation and/or deflation performance issues or difficulties.

Recall numberZ-0144-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBoston Scientific Corporation, Marlborough, MA, United States
Recall initiated2025-09-11
Classified2025-10-10
Reported by FDA2025-10-22
DistributedNationwide (US)
Countries outside the USCA
Quantity490 units
UPC / GTIN / UDI-DI00191506021412, 00191506021429, 00191506021436, 00191506021443, 00191506021450, 00191506021467, 00191506021474, 00191506021481
Lot numbers1100398489, 1100398490, 1100398491, 1100398492, 1100398493, 1100398494, 1100398495, 1100398496, 1100401206, 1100401207, 1100401208, 1100401209, 1100401210, 1100401211, 1100401212, 1100401213, 1100401214, 1100404813, 1100404814, 1100404815, 1100404816, 1100404817, 1100404818, 1100404819, 1100404820, 1100404821, 1100480113, 1100480114, 1100480115, 1100480117, 1100480622, 1100480623, 1100480624, 1100480625, 1100480626, 1100480627, 1100480628, 1100480676, 1100480677, 1100480678 and 460 more

Product

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) 72404456 (15CM IP IZ), (7) 72404457 (18CM IP IZ), (8) 72404458 (21CM IP IZ);

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0144-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.