# FDA recall Z-1834-2026

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

## Product

Medline Kits:  1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M;   2) ANGIO PACK, Model Number: DYNJT2021G;   3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B;   4) ANGIO PACK, Model Number: DYNJ51279;   5) ANGIOGRAPHY PACK II, Model Number: DYNJ52447;   6) CATH ANGIO PACK, Model Number: DYNJ53369C;   7) ANGIO PACK, Model Number: DYNJ53591A;   8) ANGIOGRAPHIC PACK, Model Number: DYNJ57516;   9) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ58722A;   10) ANGIO TRAY W/CHLORAPREP, Model Number: DYNJ62742;   11) CEREBRAL ANGIOGRAM, Model Number: DYNJ67876;   12) CSU CATH MANIFOLD KIT, Model Number: VASC1170A

## 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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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-1834-2026
- **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-1834-2026

## Citation

> AI Analytics. FDA recall Z-1834-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1834-2026. Source: US FDA. Licensed CC0.

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