# FDA recall Z-3010-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-04-08.

## Product

Medline Convenience kits labeled as:    1) CVC INSERTION PACK, Pack Number CVI4720A ;   2) CVC INSERTION PACK, Pack Number CVI4720AH;   3) CATHETER INSERTION KIT CLABSI , Pack Number CVI4880;   4) CHEST INSERTION PACK-LF , Pack Number DYNJ17634D ;   5) URETEROSCOPY, Pack Number DYNJ45882A ;   6) TONSIL PACK CATH, Pack Number DYNJ65199A ;   7) CATH PLACEMENT RIB FRACTURE , Pack Number DYNJ66475B ;   8) UROLOGY ROBOTIC PACK, Pack Number DYNJ80211C ;   9) UROLOGY ROBOTIC PACK, Pack Number DYNJ80211CH;   10) UROLOGY PK, Pack Number DYNJ80252C ;   11) PORT INSERTION PACK , Pack Number DYNJ81597

## Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-3010-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-18

- **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-3010-2024

## Citation

> AI Analytics. FDA recall Z-3010-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-3010-2024. Source: US FDA. Licensed CC0.

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