# FDA recall Z-2292-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2023-05-15.

## Product

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:    a. ART LINE KIT ICH OR, Model Number: ART900;      b. ART LINE SECUREMENT KIT W/LIDOCAINE, Model Number: DT22570;      c. ARTERIAL BUNDLE NO CATHETER, Model Number: ART995;      d. ARTERIAL LINE INSERTION KIT, Model Number: ART775B;      e. ARTERIAL LINE KIT W/O CATHETER, Model Number: ART890A;      f. ARTERIAL LINE START KIT, Model Number: ART1160;      g. ARTERIAL LINE START KIT W/O CATH, Model Number: P42453;      h. ARTERIAL LINE TRAY W/O CATHETER, Model Number: ART1180;      i. RADIAL ARTERIAL LINE KIT, Model Number: ART1070A

## Reason for recall

Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates.

## Key facts

- **Recall number:** Z-2292-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-15
- **Report date:** 2023-08-09

- **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-2292-2023

## Citation

> AI Analytics. FDA recall Z-2292-2023. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-2292-2023. Source: US FDA. Licensed CC0.

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