Data Foundry

Medical device recalls 2025

Custom Manifold Kit: REF: K09-02239C — Class II medical device recall Z-2295-2025

Ongoing recall by Merit Medical Systems, Inc., reported 2025-08-20, distributed nationwide. High pressure tubing may relax over time causing it to partially separate from the connector resulting in a vo

Recall numberZ-2295-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMerit Medical Systems, Inc., South Jordan, UT, United States
Recall initiated2025-06-05
Classified2025-08-12
Reported by FDA2025-08-20
DistributedNationwide (US)
Quantity6,327
UPC / GTIN / UDI-DI00884450204313, 00884450210000, 00884450210697, 00884450279076, 00884450279717, 00884450330043, 00884450548714, 00884450582329, 00884450640500, 00884450741146, 00884450752111, 00884450785102, 00884450860007
Lot numbersK09-10294A
Model numbersK09-02239C, K09-02249UP, K09-09110B, K09-10294A, K09-11227A, K09-11456B, K09-12123B, K09-13342AP, K09-13391BP, K09-13548, K09-14000A, K09T-12020D, K09T-12275B

Product

Custom Manifold Kit: REF: K09-02239C, K09-02249UP, K09-09110B, K09-10294A, K09-11227A, K09-11456B, K09-12123B, K09-13342AP, K09-13391BP, K09-13548, K09-14000A, K09T-12020D, K09T-12275B

Reason for recall

High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.

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-2295-2025. 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.