# FDA recall Z-2982-2024

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

## Product

Medline Convenience kits, labeled as:    1) TRACH CDS-LF  , Pack Number CDS983142B ;   2) MER TRACH CDS , Pack Number CDS984376B ;   3) Flexible LMA Pack with Syringe and Lube, Size 1, Pack Number DYND300010P;   4) Flexible LMA Pack with Syringe and Lube, Size 1.5, Pack Number DYND300015P;   5) Flexible LMA Pack with Syringe and Lube, Size 2, Pack Number DYND300020P;   6) Flexible LMA Pack with Syringe and Lube, Size 2.5, Pack Number DYND300025P;   7) Flexible LMA Pack with Syringe and Lube, Size 3, Pack Number DYND300030P;   8) Flexible LMA Pack with Syringe and Lube, Size 4, Pack Number DYND300040P;   9) Flexible LMA Pack with Syringe and Lube, Size 5, Pack Number DYND300050P;   10) TRACHEOSTOMY TRAY , Pack Number DYNDJ1061A ;   11) TRACHEOSTOMY  , Pack Number DYNJ45495F

## 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-2982-2024
- **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-2982-2024

## Citation

> AI Analytics. FDA recall Z-2982-2024. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2982-2024. Source: US FDA. Licensed CC0.

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