# FDA recall Z-3052-2024

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

## Product

Medline Convenience kits labeled as:   1) SPECIAL PROCEDURE PACK ARTERI , Pack Number 00-399024X ;  2) ARTHROSCOPY TRAY, Pack Number AM110A ;  3) HIP , Pack Number BM200A ;  4) SHOULDER ARTHROSCOPY, Pack Number BM230A ;  5) KNEE ARTHROSCOPY, Pack Number BM240A ;  6) PODIATRY PACK , Pack Number BM250A ;  7) CRANIOTOMY CDS, Pack Number CDS780025AA;  8) CRANIOTOMY CDS, Pack Number CDS780025AB;  9) CRANIOTOMY CDS, Pack Number CDS780025AC;  10) CRANIOTOMY CDS, Pack Number CDS780025X ;  11) CRANIOTOMY CDS, Pack Number CDS780025Y ;  12) LAMINECTOMY CDS-LF, Pack Number CDS780045M ;  13) LAMINECTOMY CDS-LF, Pack Number CDS780045N ;  14) LAMINECTOMY CDS-LF, Pack Number CDS780045O ;  15) CRANIOTOMY CDS, Pack Number CDS780046O ;  16) CRANI , Pack Number CDS780089V ;  17) CRANI , Pack Number CDS780089W ;  18) CRANI , Pack Number CDS780089X ;  19) CRANIOFACIAL CDS, Pack Number CDS780102K ;  20) CRANIOFACIAL CDS, Pack Number CDS780102L ;  21) TRAUMA/LIVER CDS-LF , Pack Number CDS780104L ;  22) CRANIO

## 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-3052-2024
- **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-3052-2024

## Citation

> AI Analytics. FDA recall Z-3052-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-3052-2024. Source: US FDA. Licensed CC0.

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