# FDA recall Z-2167-2023

> **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)	ARTERIAL BUNDLE NO CATHETER, Model Number ART995;  b)	ART LINE KIT NO CATH, Model Number ARTNC145;  c)	CENTRAL LINE TRAY, Model Number CVI4705;  d)	CENTRAL LINE INSERTION PACK, Model Number CVI4805;  e)	ED CENTRAL LINE KIT, Model Number CVI4865;  f)	NO CATH MIDLINE INSERTION KIT, Model Number CVI4950A;  g)	CENTRAL LINE PROCEDURE KIT, Model Number DT22260;  h)	ADULT EPIV INSERTION TRAY, Model Number DYNDA2482;  i)	ULTRASOUND GUIDED PIV KIT, Model Number DYNDA2669;  j)	I.R. PICC PACK, Model Number DYNDA2759;  k)	IR SONO PACK, Model Number DYNDA3010;  l)	NEONATAL PICC LINE TRAY, Model Number DYNDC2120B;  m)	PICC SUPPLEMENTAL KIT, Model Number DYNDC2373A;  n)	CENTRAL LINE KIT, Model Number DYNDC2582A;  o)	CENTRAL LINE KIT UTMB, Model Number DYNDC3061;  p)	FNA TRAY, Model Number DYNDH1123B;  q)	CVL PACK, Model Number DYNJ00281O;  r)	CENTRAL VENOUS ACCESS PACK-LF, Model Number DYNJ0214541O;  s)	CENTRAL 

## 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-2167-2023
- **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-2167-2023

## Citation

> AI Analytics. FDA recall Z-2167-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2167-2023. Source: US FDA. Licensed CC0.

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