# FDA recall Z-2179-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2023-05-18.

## Product

Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following:   a)	NO-CATH RADIAL ARTERIAL PREMIU, Model Number ARTNC115;  b)	MAJOR VASCULAR, Model Number CDS980752I;  c)	PICC LINE DOUBLE LUMEN CDS, Model Number CDS982858F;  d)	PICC LINE TRIPLE LUMEN CDS, Model Number CDS982859F;  e)	CHP TRANSPLANT CDS, Model Number CDS983082J;  f)	CLOSURE CDS, Model Number CDS983704I;  g)	MIDLINE INSERTION TRAY, Model Number CVI4340;  h)	PORT INSERTION PACK, Model Number CVI4765;  i)	MAX BARRIER KIT, Model Number DYND2673B;  j)	POWERGLIDE PLACEMENT KIT, Model Number DYNDA1468C;  k)	DEPIPPO PACK, Model Number DYNDA2011B;  l)	VEIN PROCEDURE KIT, Model Number DYNDA2076;  m)	SCLEROTHERAPY KIT, Model Number DYNDA2148A;  n)	IR SONO PACK, Model Number DYNDA2365B;  o)	ULTRASOUND BASIC KIT, Model Number DYNDC2099;  p)	PIV WITH ULTRASOUND KIT, Model Number DYNDC2399A;  q)	PARA THORACENTESIS TRAY, Model Number DYNDH1165A;  r)	ULTRASOUND TRAY, Model Number DYNDH1204;  s)	PARA/THORACENTESIS

## Reason for recall

Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

## Distribution

Worldwide Distribution: US (Nationwide) and OUS (foreign) United Arab Emirates, Singapore, Lebanon, China Qatar, Costa Rica, India, Canada, Panama & Saudi Arabia.

## Key facts

- **Recall number:** Z-2179-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-18
- **Report date:** 2023-07-26

- **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-2179-2023

## Citation

> AI Analytics. FDA recall Z-2179-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2179-2023. Source: US FDA. Licensed CC0.

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