# FDA recall Z-1842-2026

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

## Product

Medline Kits:  1) NEWBORN ADMISSION, Model Number: DYKB1038;   2) DRAINAGE TRAY, Model Number: DYNDA3188;   3) VA ORLANDO SHOULDER PACK, Model Number: DYNJG001027B;   4) TUMESCENT SYRINGE KIT, Model Number: DYNJTUMSYR;   5) OMC PTCA PACK, Model Number: DYNJT3719;   6) PORT PACK, Model Number: DYNJT5667;   7) WASTE MANAGEMENT KIT - 2, Model Number: DYNJWASTEKIT2;   8) CARDIAC CATH, Model Number: DYNJ20175J;   9) D&C PACK-POB, Model Number: DYNJ33521D;   10) BASIC PACK, Model Number: DYNJ38533F;   11) CATH PACK IMPLANT, Model Number: DYNJ39230D;   12) CERVICAL SPINE PACK, Model Number: DYNJ40886B;   13) MV-IR ANGIO DRAPE PACK-LF, Model Number: DYNJ41553F;   14) TV ENDOVASCULAR-LF, Model Number: DYNJ41558D;   15) MAJOR PACK-LF, Model Number: DYNJ44816J;   16) ANGIOGRAPHY PACK, Model Number: DYNJ48683A;   17) EXTREMITY PACK, Model Number: DYNJ55922C;   18) NEURO PACK, Model Number: DYNJ57785C;   19) PACEMAKER PACK, Model Number: DYNJ61377B;   20) VASCULAR PACK, Model Number: DYNJ62683D;   

## 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1842-2026
- **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-1842-2026

## Citation

> AI Analytics. FDA recall Z-1842-2026. Retrieved 2026-09-07 from https://api.ai-analytics.org/recall/Z-1842-2026. Source: US FDA. Licensed CC0.

---

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