Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1431-2025 — namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. , REF 60010511; 3) MTS,LT,HT,KIT-BRYAN,LGH,M.C.,EAST, REF 60020323; 4) MTO,RIGHT,KIT-BRONSON,M* HOSP PG, REF 60020676; 5) MTS,LEFT HEART,KIT-C*,MEM HLTHCARE, REF 6003

U.S. FDA — Device Enforcement · United States · 2025-02-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1431-2025
Date of alert: 2025-02-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: MEDLINE INDUSTRIES, LP - Northfield
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10193489040319

Reported risk: The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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