# FDA recall Z-2156-2023

> **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)	BLOCK PACK, Model Number DYNJ81722;   b)	PAIN BLOCK TRAY, Model Number DYNJRA0827A;   c)	PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881;   d)	PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881A;   e)	PAIN TRAY, Model Number DYNJRA1603;   f)	FEMORAL BLOCK TRAY, Model Number DYNJRA1739A;   g)	TAP BLOCK, Model Number DYNJRA1823;   h)	NERVE BLOCK PREP TRAY, Model Number DYNJRA1837;   i)	PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1847;   j)	ANESTHESIA BLOCK PACK - TBR, Model Number DYNJRA1864;   k)	18G CPNB 20G STYLETED CATHETER, Model Number DYNJRA1869;   l)	NERVE BLOCK TRAY, Model Number DYNJRA1878;   m)	BLOCK KIT, Model Number DYNJRA1893;   n)	NERVE BLOCK TRAY, Model Number DYNJRA1900;   o)	US TPI KIT, Model Number DYNJRA1945;   p)	PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA1975;   q)	DR LEWIS US TRAY, Model Number DYNJRA1998;   r)	ULTRASOUND GUIDED NERVE BLOCK, Model Number DY

## 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-2156-2023
- **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-2156-2023

## Citation

> AI Analytics. FDA recall Z-2156-2023. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-2156-2023. Source: US FDA. Licensed CC0.

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