# FDA recall Z-2293-2023

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2023-05-15.

## Product

Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel.  Labeled as the following:    a.18G CPNB 20G STYLETED CATHETER, Model Number: DYNJRA1869;      b. ACUTE PAIN BLOCK TRAY, Model Number: DYNJRA0949C;      c. ANESTHESIA BLOCK KIT, Model Number: DYNJRA1864;      d. BLOCK KIT, Model Number: DYNJRA1893;      e. DR LEWIS US TRAY, Model Number: DYNJRA1998;      f. ECHOGENIC SINGLE SHOT TRAY, Model Number: DYNJRA1978, DYNJRA1978A, SAMPA0109;      g. FEMORAL BLOCK TRAY, Model Number: DYNJRA1739A;      h. NERVE BLOCK INSERTION, Model Number: DYNJRA2027;      i. NERVE BLOCK PREP TRAY, Model Number: DYNJRA1837;      j.  NERVE BLOCK TRAY, Model Number: DYNJRA1878, DYNJRA1900;     k.  NERVE PERIPHERAL PACK, Model Number: DYNJRA2055;      l. PAIN BLOCK TRAY, Model Number: DYNJRA0827A;      m. PAIN PREP TRAY W/PROBE COVER, Model Numbers: DYNJRA0881, DYNJRA1847, DYNJRA1975;     n. PAIN PREP W/ PROBE COVER TRAY, Model Number: DYNJRA2028;     o. PAIN PREP W/PROBE COVER TRAY

## Reason for recall

Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, China, Costa Rica, India, Lebanon, Panama, Qatar, Saudi Arabia, Singapore, United Arab Emirates.

## Key facts

- **Recall number:** Z-2293-2023
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-15
- **Report date:** 2023-08-09

- **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-2293-2023

## Citation

> AI Analytics. FDA recall Z-2293-2023. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-2293-2023. Source: US FDA. Licensed CC0.

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