# FDA recall Z-2295-2023

> **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. ANGIOGRAM TRAY, Model Number: DYNJ33638J;      b. BLOCK TRAY, Model Number: DYNJRA1543;     c. BMT- NERVE PERIPH PK, Model Number: DYNJRA1247;      d. CVOR ANGIOGRAPHY PACK-LF, Model Number: DYNJ42367B;      e. FEMORAL BLOCK TRAY, Model Number: DYNJRA1739;      f. NERVE BLOCK ACCESSORY PACK, Model Number: DYNJ0134147D;      g. NERVE BLOCK PREP TRAY, Model Numbers: DYNJRA1220, DYNJRA1571;      h. NERVE BLOCK SUPPORT TRAY, Model Number: DYNJRA1109A;      i. NERVE BLOCK TRAY, Model Numbers: DYNJRA0656A, DYNJRA1287A, DYNJRA1604;     j. NERVE BLOCK TRAY/PREFERRED, Model Number: DYNJRA0725;      k. PK, RADIOLOGY-NEURO-IR, Model Number: DYNJ51107B;      l. SINGLE SHOT NERVE BLOCK TRAY, Model Number: DYNJRA1773;      m. ULTRASOUND BLOCK PREP TRAY, Model Number: PAIN1622A;      n. UNIVERSAL BLOCK TRAY/2, Model Number: DYNJRA1635A;

## 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-2295-2023
- **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-2295-2023

## Citation

> AI Analytics. FDA recall Z-2295-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2295-2023. Source: US FDA. Licensed CC0.

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