# FDA recall Z-1431-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-02-12.

## Product

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 60035977;   6) MTS,LEFT HEART,KIT,J*,M*,C*, REF 60040273;   7) MTS,LEFT HEART,KIT,C*,C*, REF 60100313;   8) MTS,3V,KIT-M*,MEMORIAL, REF 60131208;   9) MTS,3V,KIT-M*,MEMORIAL, REF 60131208;   10) MTO,LEFT HEART,KIT,-,N* HOSPITAL PG, REF 60140101;   11) MTO,LEFT HEART,KIT,-,N* HOSPITAL PG, REF 60140101;   12) MTS,LEFT HEART,MAN,KIT,S*-BALTIMORE, REF 60190947;   13) MTS-LEFT HEART,KIT-W*,H* HOSP PG, REF 60231052;   14) MTO,3-VALVE,KIT-T*,A*-PG, REF 65190182;   15) MTO,LEFT HEART,KIT,-,S* F*,-,PG, REF 65190474;   16) MTS,DR.,MCKAYS,4V,KIT,-,H* HOSP PG, REF 600800516;   17) MTS,EP,KIT,-,S*,TEACHING HOSPITAL PG, REF 601309013;   18) MTS,RHT,HRT-S* HOSP &,MC, REF 601905413;   19) MTS,PEDS,LFT,&,RT,HRT-

## Reason for recall

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

## Distribution

Worldwide distribution - US Nationwide and the countries of The Netherlands, New Zealand, Slovakia

## Key facts

- **Recall number:** Z-1431-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-12
- **Report date:** 2025-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1431-2025

## Citation

> AI Analytics. FDA recall Z-1431-2025. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-1431-2025. Source: US FDA. Licensed CC0.

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