# FDA recall Z-2997-2024

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

## Product

Medline Convenience kits labeled as:   1) PUNCTURE TRAY , Pack Number 00-401649G ;  2) PICC LINE TRAY, Pack Number 00-401993O ;  3) ARTERIOGRAM TRAY, Pack Number 00-402001T ;  4) ARTERIOGRAM TRAY, Pack Number 00-402001U ;  5) HEALTH LINE MAX BARRIER KIT , Pack Number A134-MAX ;  6) ART-LINE SURGERY PACK-LF, Pack Number ARTNC175 ;  7) AV FISTULA PACK , Pack Number CDS840188M ;  8) VP SHUNT, Pack Number CDS840193V ;  9) THROMBECTOMY/AV FISTULA CDS-LF, Pack Number CDS840295G ;  10) IVC PLACEMENT CDS-LF, Pack Number CDS860033A ;  11) IVC PLACEMENT CDS-LF, Pack Number CDS860033AH;  12) CENTRAL LINE CDS, Pack Number CDS930092V ;  13) CENTRAL LINE CDS, Pack Number CDS930092W ;  14) CENTRAL LINE CDS, Pack Number CDS930092X ;  15) C LINE INSERTION CDS, Pack Number CDS980379I ;  16) C LINE INSERTION CDS, Pack Number CDS980379J ;  17) AV FISTULA - SMH, Pack Number CDS980916L ;  18) AV FISTULA CDS, Pack Number CDS981513G ;  19) VASCULAR ACCESS CDS , Pack Number CDS981552F ;  20) VP SHUNT CDS, Pack

## 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-2997-2024
- **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-2997-2024

## Citation

> AI Analytics. FDA recall Z-2997-2024. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2997-2024. Source: US FDA. Licensed CC0.

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