# FDA recall Z-2184-2023

> **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)	LACERATION TRAY, Model Number DYNDL1134A;   b)	ULTRASOUND GUIDED IV/MIDLINE K, Model Number DYNDV2385;   c)	PEDIATRIC CENTRAL LINE KIT, Model Number DYNJ38885B;   d)	CENTRAL LINE TRAY, Model Number DYNJ42902B;   e)	CENTRAL LINE PACK - COMPANION, Model Number DYNJ47215D;   f)	PICC LINEPACK (PCLUI)642-LF, Model Number DYNJ47717A;   g)	PK CUST CENTRAL LINE PACK, Model Number DYNJ60586;   h)	TUNNEL LINE PACK, Model Number DYNJ67990;   i)	CLOSURE PACK, Model Number DYNJ83054A

## 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-2184-2023
- **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-2184-2023

## Citation

> AI Analytics. FDA recall Z-2184-2023. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2184-2023. Source: US FDA. Licensed CC0.

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