# FDA recall Z-0991-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class I · device recall initiated 2024-12-31.

## Product

Medline General Surgery Tray Kits:     1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B;  2) ARTERIAL LINE BUNDLE, Item Number ART255;  3) ARTERIAL LINE TRAY, Item Number ART350;  4) ARTERIAL LINE BUNDLE, Item Number ART355;  5) ARTERIAL LINE BUNDLE, Item Number ART355 ;  6) ARTERIAL LINE INSERTION TRAY, Item Number ART475;  7) ARTERIAL LINE BUNDLE - OR, Item Number ART535A;  8) ARTERIAL LINE TRAY, Item Number ART545A;  9) ARTERIAL LINE INSERTION KIT, Item Number ART775C;  10) ARTERIAL LINE TRAY, Item Number ART840;  11) ARTERIAL LINE KIT, Item Number ART890B

## Reason for recall

The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

## Distribution

US Nationwide.

## Key facts

- **Recall number:** Z-0991-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-31
- **Report date:** 2025-02-05

- **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-0991-2025

## Citation

> AI Analytics. FDA recall Z-0991-2025. Retrieved 2026-08-03 from https://api.ai-analytics.org/recall/Z-0991-2025. Source: US FDA. Licensed CC0.

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