---
title: "namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF ... — FDA record Z-1431-2025 | Is It on Recall"
description: "The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway."
url: https://isitonrecall.com/recall/fda-device-z-1431-2025-namic-convenience-kits-labeled-as-1-mts-4-valve-lft-hrt-kit-ahs-a-nw-ref-60010468-2-mts-right-heart/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A\*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS... — FDA record Z-1431-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 12, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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-S\* HOSP, REF 601905414; 20) MTO,SCH,BEL,J\*,H\*-ST-PAUL,-,PG, REF 606604328; 21) LHK,-,MID,3VCOMP,OFF,PS,S10RA, REF 613000122; 22) MTS,LHK,W\* HOSPITAL, REF 6010034281; 23) MTS,LHK,W\* HOSPITAL, REF 6010034281; 24) MTS,LHK,P\*,P\* MED CTR, REF 6010171931; 25) MTS,LHK,M\* HEALTHCARE,MGMT, REF 6061073001; 26) TVR US B\* INTEGRATED SERVICE CENT, REF 601316711A; 27) LHK-S\* MEDICAL CENTER,A\*, REF 60190776A; 28) LHK,-,S\*,AND,W\* HOSPITAL, REF 60191118A.
- **Reason**: The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 1669 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1431-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1431-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 1) REF60010468, UDI/DI 10193489040319 (each) 20193489040316 (case), Lot Number 0000140099; 2) REF60010511, UDI/DI 10193489040357 (each) 20193489040354 (case), Lot Number 0000141267; 3) REF60020323, UDI/DI 10193489041071 (each) 20193489041078 (case), Lot Number 0000139976; 4) REF60020676, UDI/DI 10193489041200 (each) 20193489041207 (case), Lot Number 0000140410; 5) REF60035977, UDI/DI 10193489042672 (each) 20193489042679 (case), Lot Number 0000140081; 6) REF60040273, UDI/DI 10193489042832 (each) 20193489042839 (case), Lot Number 0000140896; 7) REF60100313, UDI/DI 10193489045048 (each) 20193489045045 (case), Lot Number 0000140520; 8) REF60131208, UDI/DI 10193489046762 (each) 20193489046769 (case), Lot Number 0000140075; 9) REF60131208, UDI/DI 10193489046762 (each) 20193489046769 (case), Lot Number 0000140364; 10) REF60140101, UDI/DI 10193489047868 (each) 20193489047865 (case), Lot Number 0000139979; 11) REF60140101, UDI/DI 10193489047868 (each) 20193489047865 (case), Lot Number 0000140016; 12) REF60190947, UDI/DI 10193489050677 (each) 20193489050674 (case), Lot Number 0000140835; 13) REF60231052, UDI/DI 10193489053203 (each) 20193489053200 (case), Lot Number 0000140045; 14) REF65190182, UDI/DI 10193489063028 (each) 20193489063025 (case), Lot Number 0000140258; 15) REF65190474, UDI/DI 10193489063059 (each) 20193489063056 (case), Lot Number 0000141271; 16) REF600800516, UDI/DI 10193489070347 (each) 20193489070344 (case), Lot Number 0000140829; 17) REF601309013, UDI/DI 10193489071054 (each) 20193489071051 (case), Lot Number 0000139959; 18) REF601905413, UDI/DI 10193489072099 (each) 20193489072096 (case), Lot Number 0000139674; 19) REF601905414, UDI/DI 10193489072105 (each) 20193489072102 (case), Lot Number 0000139097; 20) REF606604328, UDI/DI 10193489073898 (each) 20193489073895 (case), Lot Number 0000140043; 21) REF613000122, UDI/DI 10193489074482 (each) 20193489074489 (case), Lot Number 0000140963; 22) REF6010034281, UDI/DI 10193489095951 (each) 20193489095958 (case), Lot Number 0000139656; 23) REF6010034281, UDI/DI 10193489095951 (each) 20193489095958 (case), Lot Number 0000140079; 24) REF6010171931, UDI/DI 10193489104943 (each) 20193489104940 (case), Lot Number 0000140976; 25) REF6061073001, UDI/DI 10193489095692 (each) 20193489095699 (case), Lot Number 0000140936; 26) REF601316711A, UDI/DI 10197344028696 (each) 20197344028693 (case), Lot Number 0000139675; 27) REF60190776A, UDI/DI 10193489148763 (each) 20193489148760 (case), Lot Number 0000140484; 28) REF60191118A, UDI/DI 10193489180657 (each) 20193489180654 (case), Lot Number 0000139969. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New Mexico](https://isitonrecall.com/state/new-mexico/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
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- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 2, 2025
- **Recall initiation date**: Feb 12, 2025
- **Center classification date**: Mar 21, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1431-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)
