# FDA recall Z-1836-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-02-25.

## Product

Medline Kits:  1) MTS LEFT HEART KIT-CAROLINAS HOS, Model Number: 60021775;   2) DBD-MTS LHK BHS BAPTIST. LOUISVI, Model Number: 60022026;   3) MTO LEFT HEART KIT SUMMA BARBERT, Model Number: 60022673;   4) MTS LH KIT-UNIV OF MIAMI PG, Model Number: 60030817;   5) MTS LEFT HEART KIT SPRINGFIELD R, Model Number: 60031245;   6) MTS PERIPHERAL KIT SPRINGFIELD R, Model Number: 60031247;   7) MTS LEFT HEART KIT-COLISEUM MED, Model Number: 60031928;   8) MTS LEFT HEART KIT -2-CALIFORNIA, Model Number: 60033011;   9) MTS LEFT HEART KIT JOHN MUIR CON, Model Number: 60040273;   10) MTS EP MANIFOLD KIT TEXAS HLTH P, Model Number: 60041268;   11) MTS 3V MANIFOLD KIT-SPARROW HOSP, Model Number: 60050097;   12) MTS LEFT HEART KIT FORT SANDERS, Model Number: 60060387;   13) MTS LEFT HEART KIT-GOOD SAMARITA, Model Number: 60070435;   14) DBD-MTS ANGIO KIT-MOUNT HOOD MED, Model Number: 60070521;   15) MTS LFT HRT KIT-GRAND VIEW PG, Model Number: 60071743;   16) MTS CUSTOM MANIFOLD KIT-INGALLS, Model N

## Reason for recall

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1836-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-25
- **Report date:** 2026-04-29

- **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-1836-2026

## Citation

> AI Analytics. FDA recall Z-1836-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1836-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*