# FDA recall Z-2770-2024

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

## Product

Centurion procedure kits labeled as:    1) BONE MARROW TRAY, Pack Number SPEC0255;   2) CT/ULTRASOUND BIOPSY, Pack Number SPEC0262;   3) FINE LACERATION KIT, Pack Number SUT17215;   4) INFECTION DRIVELINE MANAGEMENT KIT, Pack Number DM645;   5) LACERATION TRAY, Pack Number DYNDL1159B;   6) SUTURE TRAY, Pack Number DYNDS1064B

## 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

## Key facts

- **Recall number:** Z-2770-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-04

- **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-2770-2024

## Citation

> AI Analytics. FDA recall Z-2770-2024. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2770-2024. Source: US FDA. Licensed CC0.

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