# FDA recall Z-2172-2023

> **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)	CHP COCHLEAR SUPPLEMENT CDS, Model Number CDS983069I;   b)	HEAD AND NECK PACK, Model Number DYNJ30245;   c)	IR THYROID PACK (THLUF)642-LF, Model Number DYNJ47716B;   d)	CENTRAL LINE INSERTION, Model Number DYNJ63347A;   e)	TAVR FAIRFAX, Model Number DYNJ63634A;   f)	PARATHYROID PACK, Model Number DYNJ81389A;   g)	THYRIOD PACK, Model Number DYNJ83960;   h)	WMC COCHLEAR IMPLANT ADD ON, Model Number DYNJ907206D

## 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-2172-2023
- **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-2172-2023

## Citation

> AI Analytics. FDA recall Z-2172-2023. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-2172-2023. Source: US FDA. Licensed CC0.

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